Executive Director of Patient Safety and Quality
Associate director job in Bethesda, MD
Partners with the JHM VP of Safety and Quality to support the health system goals of eliminating preventable harm, continuously improving patient outcomes and patient/family experience, reducing waste/cost in healthcare delivery and achieving health equity. Supports external reporting to achieve national leader performance and minimize financial risk in pay for performance programs. Works collaboratively with entity and health system leaders, clinical departments, service lines and external experts to improve patient outcomes and ensure the highest performance.
Role Accountabilities Include:
In collaboration with the JHHS VP of Safety and Quality, system and entity leaders, recommends strategic objectives for improving quality processes and outcomes, safety, equity and value that align with the national leader strategy and JHM strategic plan.
Develops comprehensive strategic and tactical plans to achieve JHM, JHHS and Armstrong Institute goals and priorities.
Partners to ensure a reliable, timely and streamlined safety and quality reporting system to provide clinical and administrative leadership with the information necessary to monitor performance.
Partners to establish appropriate indicators, ensure that they are monitored, and assess for continuous improvement.
Supports entity leaders to ensure that all external regulatory requirements are met or exceeded.
Serves as liaison for quality and safety performance and initiatives with federal/state regulatory agencies, clinicians, leadership and external experts.
Identifies, leads and supports interdisciplinary efforts in clinical transformation to eliminate preventable harm, improve patient outcomes and experience, reduce waste and ensure equity across the continuum of care.
Initiatives, oversees and integrates comprehensive safety and quality programs.
Establishes strong linkages with key stakeholders for patient safety and quality across the health system.
Qualifications:
Master's degree in healthcare, business administration or related field.
5 years of management experience.
10 years of relevant healthcare experience.
Experience leading patient safety and quality.
Knowledge and experience in healthcare delivery, patient safety, healthcare quality, performance improvement, healthcare regulation, pay for performance, and public reporting.
Demonstrated ability to lead to impact patient safety and quality outcomes.
Experience in a health system leadership role preferred
Employees who are clinical are required to have a license in the State of Maryland as a Registered Nurse (RN), Pharmacist, a Medical Doctor (MD), a Doctor of Osteopathy (DO), or a Physician Assistant (PA), for
example.
National certification in patient safety and/or healthcare quality
Executive Director of Finance
Associate director job in Baltimore, MD
Job Responsibilities:
The Executive Director of Finance oversees Johns Hopkins Bayview Medical Center (“JHBMC”) financial operations under the direction of the JHBMC Vice President of Finance/CFO. This position will provide strategic leadership and direction for all financial aspects within the functional area, and will provide senior management with financial reports and overall financial management necessary for the fiscally prudent operation of each area. The position will be an integral part of the management of the functional area and will ensure development of a strong finance team through the mentoring of key individuals within the department.
Role Accountabilities Include
Development and review of the functional area(s)' finance staff
Partner with operational leaders to assess, analyze and help manage operating and capital budgets. Opine on business plans, particularly on the revenue assumptions and bottom line impact of regulated services under GBR.
Provide financial guidance and consultation to senior management and key stakeholders
Annual operating and capital budgets
Financial analysis of actual and budgeted performance
Providing monthly accruals and budget variance explanations to General Accounting
Assist with production and maintenance of the monthly financial statements and reports
Assist with revenue reconciliation, billing, and charge entry
Research project administration and accounting (including grant submissions, effort reporting, and cost transfers)
Partner with key stakeholders across the Johns Hopkins Health System to achieve strategic and operational objectives
Responsible for using a data driven approach to assess new opportunities in the context of market demand and financial/resource investment feasibility
Program/product development analysis
Develop and/or monitor compliance with financial policies, internal controls, and internal audit recommendations
Oversee budget development for JHBMC under the scope of the functional area assigned ensuring that the combined whole is accurate and complete. Monitor and address budget variances
HBMC oversight of regionalized financial functional areas
Develop and enforce departmental financial policies and internal controls. Work independently with limited supervision.
Manages staff and has responsibility for hiring, firing, and performance management
Resolve issues that block process; Identify appropriate communication channels; Primary responsibility for financial issues of JHBMC; Must ensure accuracy of data and quality of service. Utilize techniques of financial analysis to identify, plan, develop, implement and monitor financial strategies and resolutions to problem areas
Develop and interpret a variety of financial reports which may include: Income statements, balance sheets, statement of cash flows; Ratio interpretation, financial performance monitoring as well as prospective external partners
Qualifications:
BS/BA in Accounting, Finance, or related field required. CPA or Master's degree strongly preferred.
Minimum ten years progressive experience in Business and Finance preferably in an academic medical center. 5-7 years of management experience with significant business impact.
Working understanding of HSCRC payment policies and compliance requirements
COO
Associate director job in Maryland
Full-time Description
Do you thrive on turning vision into action and helping teams succeed together? Are you passionate about building strong operations while honoring the people who make the work possible? Do you bring a balance of strategy and hands-on leadership, ready to step into the field as easily as the boardroom? If you are a decisive, collaborative leader who values curiosity and learning as much as results, we want to talk to you!
Our ideal COO is:
•Transparent Communicator - You share direction clearly, encourage dialogue at every level, and listen actively to ensure understanding across the organization.
•Hands-On Leader - You're not confined to an office; you work shoulder to shoulder with the team, respecting every role and valuing the contributions of all employees.
•Curious and Humble - You ask thoughtful questions, observe before acting, and learn from the people around you. You avoid preconceived ideas and adapt by truly understanding how the business operates.
•Accountable and Decisive - You own outcomes, make timely, data-driven decisions without analysis paralysis, and instill confidence by following through from start to finish.
•Strategic Business Partner - You bring strong business acumen, guiding growth, financial health, and long-term planning while championing innovation.
•Empathetic Mentor - You coach and develop talent, celebrate wins, and foster a culture of integrity, humility, and respect.
Our ideal COO combines vision with curiosity, grit with humility. This is a leader who drives results while honoring the heritage of a family-owned business. You'll enhance processes, shape growth, and create harmony between people and performance. At Mid Atlantic Contracting, your leadership will have a direct impact on scaling the company, supporting employees, and building a future where success is shared by all.
RESPONSIBILITIES
The responsibilities of the COO role include, but are not limited to:
Executive Leadership
•Guide the organization toward growth by translating strategic goals into a clear direction.
•Champion a collaborative, team-first environment rooted in respect and accountability.
•Inspire confidence through decisive action and consistent follow-through.
•Foster innovation and process improvement while preserving the company's values.
Management
•Oversee financial performance across the enterprise, including P&L and pro forma planning.
•Strengthen client retention, satisfaction, and acquisition through operational excellence.
•Lead employee growth and retention efforts by mentoring, coaching, and building efficiencies.
•Design and implement effective processes, tools, and metrics for proper labor and staffing levels.
•Manage multiple verticals and divisions, ensuring alignment and clarity across teams.
•Support and manage sales leaders in driving organizational revenue and market expansion.
Accountability
•Hold teams responsible for process adoption and execution.
•Address escalated issues with fairness and clarity, serving as a sounding board and problem-solver.
•Ensure operational initiatives are carried through from concept to completion.
•Balance financial stewardship with people-first decision making.
•Make work engaging and rewarding, reinforcing the company's passion for winning together.
**This is a full-time, in-person position based in the Woodbine, MD area**
Apply through the link: *********************************************************************************
Requirements
QUALIFICATIONS
Required
•Minimum 5 years in an executive-level role such as COO, VP of Operations, or Director of Operations.
•Experience leading multiple divisions concurrently.
•Experience in a blue-collar service industry, managing diverse teams from hourly field staff to formally trained white-collar professionals.
•Commercial construction background, including fleet, safety programs, purchasing and facilities management.
•Proven financial planning and analysis expertise with P&L management and strategic opportunity development.
•Track record managing sales professionals and organizational growth of $20M-$50M in revenue.
Preferred
•Career progression from field experience into leadership, demonstrating steady growth and success.
•Exposure to light manufacturing.
•Background in privately held or family-owned businesses.
•Enterprise risk management knowledge, including insurance, bonding, and HR risk oversight.
•Experience guiding growth from $20M-$100M in revenue.
•Involvement in merger and acquisition integration.
•Government contracting experience.
Desired
•Exposure to multiple trades, including general contracting, wireless infrastructure, concrete contracting, metal fabrication and contract manufacturing.
•Experience scaling organizations from 10 employees to 500 employees.
Salary Description $180,000-$210,000
Associate Director, Field Strategy, Nephrology
Associate director job in Annapolis, MD
**Associate Director, Field Strategy, Nephrology/Immunology** The **Associate Director, Field Strategy** plays a critical role in enabling **sales execution** by ensuring that field teams have the **clarity, insights, and tools** needed to drive performance. This role is responsible for aligning **key metrics and insights** **with brand strategy** , ensuring that analytics dashboards and reporting tools provide **actionable, field-relevant intelligence** - ensures insights are turned into action.
Rather than creating new tools, data, or systems, this individual **orchestrates the seamless integration and application** of existing resources, ensuring field teams can focus on **flawless execution of sales strategy** . They ensure field teams are fully informed, equipped, and leveraging all available tools, insights, and strategic initiatives to maximize impact.
This position provides **strategic support across multiple regions** , partnering closely with **sales leadership nationwide** to ensure a broad perspective on **performance trends and execution effectiveness** . Additionally, the role collaborates with **Business Analysis team** to ensure field teams have access to **actionable insights and a consistent reporting framework** that drives informed decision-making at a national, regional, and territory level.
**Key responsibilities:**
+ **Define & Measure Field Impact:**
+ Establish **KPIs** that align with brand strategy to measure the field's effectiveness in driving business outcomes.
+ Develop **frameworks** to assess whether field teams are successfully executing strategic priorities
+ **Standardize Performance Tracking & Reporting**
+ Ensure **consistency in national and subnational tracking** of field performance and execution through standardized dashboards.
+ Partner with Commercial Operations to **streamline reporting processes** and provide clear, actionable insights
+ **Drive Strategic Clarity and Field Engagement & Execution**
+ Ensure that **brand strategy is effectively translated into field execution** , with clear expectations at the national, regional, ecosystem, and territory levels
+ Act as a strategic partner to sales leadership, ensuring that field insights inform future strategic decisions
+ Ensure field teams understand the **"why" behind initiatives** , fostering strong alignment with broader commercial objectives.
+ **Lead Business Review Framework & Execution**
+ Own the **business review process framework** , ensuring a standardized approach that addresses key strategic questions from senior leadership.
+ Develop clear templates and storytelling approaches to ensure **business reviews provide meaningful insights and drive decision-making**
+ **Support Business & Account Planning**
+ Ensure that **business and account plans are created effectively** and that key stakeholders (e.g., SBDs, ELs, HSAs) are accountable for execution.
+ Monitor plan execution and provide feedback to optimize performance at all levels
+ **Compliance Management:**
+ Must comply with all state and federal laws, regulations and guidelines including PhRMA Code on Interactions with Healthcare Professionals as well as complying with all OAPI standards and policies relating to all job activities
**Qualifications**
+ Bachelor's degree required; MBA or advanced degree preferred.
+ Minimum of 7 years of pharmaceutical experience
+ Prior experience in field leadership roles such as first or second line leadership, regional operational and customer strategy roles or other field-based support roles preferred
+ Proven experience in data analysis, business intelligence, and strategic planning within a pharmaceutical sales environment
+ Strong ability to distill data into concise, actionable insights to drive business performance
+ Excellent communication and stakeholder engagement skills, with the ability to influence and align across multiple teams
Proven ability to collaborate with cross
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $153,700.00 - Maximum $229,770.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Associate Director, Global Submission Management
Associate director job in Baltimore, MD
At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.
The Associate Director of Global Submission Management (GSM) is responsible for leading, managing, strategizing, and overseeing the planning, preparation, coordination, and delivery of global regulatory submissions in compliance with applicable regulations and standards. This role involves providing hands-on operational support for submission activities while ensuring strategic alignment and process optimization across different regions. It also includes resource planning, budgeting, vendor management, and technical oversight to support the objectives of Global Regulatory Operations. The Associate Director will collaborate with the Heads of Submissions Management for the EU and Japan as needed and utilize "Follow-the-sun" processes to ensure submission timelines are met regardless of the region.
The Associate Director, Global Submission Management (GSM, is responsible for the effective operation of Global Submission projects, ensuring the consistent application of global procedures and standards, and proactively assessing process performance for necessary optimizations. The Associate Director serves as the primary liaison between R&D functions, acting as the submission lead for designated global applications (e.g., INDs, NDAs, MAAs, supplements, amendments, and variations), to facilitate cross-functional logistics and communication that support submission planning. This role provides submission leadership by managing the operational aspects of global regulatory submissions to produce high-quality, time-sensitive deliverables in accordance with agreed-upon submission timelines. Additionally, the AD oversees the process for creating and updating the Global Regulatory Operations Submission Content Plan (GSCP) for major regulatory submission final deliverables, ensuring compliance with applicable regulatory agency regulations, guidelines, and specifications (e.g., FDA, EMA, HC, PMDA, Emerging Markets, ICH, CDISC) within defined timelines.
Essential Functions:
Leadership and Strategy
* Provides leadership for the Global Submissions Team ensuring projects are appropriately resourced, partnering with other regional Submission Heads for additional support for resources when needed.
* Provides the Regulatory Submission Management for a lead compound or submission project that has been identified as critical to Eisai's business success.
* Provides management oversight for the Global Submission Management department, supporting the generation, and when necessary, the re-engineering of Eisai "Best Practices" related to global submission management and dossier development in pursuit of optimal processing performance while maintaining full compliance with Health Authority requirements and guideline.
Global Collaboration
* Collaborates with the EU and Japan Heads of Submission Management to optimize resource allocation and implement "follow-the-sun" workflows for timely submissions across all regions.
* Foster strong cross-regional communication and collaboration to support global objectives.
* Promotes a culture of performance and teamwork, with a focus on staff development in technical skills, interpersonal skills, education, and training, enhancing competency and professionalism.
* Maintains visibility within the organization by regularly presenting on various GSM-related topics. This includes showcasing the achievements, ongoing projects, and developments of the GSM organization, as well as emerging trends in eCTD regulatory submissions. Additionally, cultivate positive and constructive relationships with other members of the Global Regulatory Operations (GRO) team and regulatory colleagues.
* Actively participates in agency/industry events regularly, staying abreast of current developments, trends, and technologies, fostering constructive business relations with other industry peers, Health Authority representatives, and critical business partners/vendors.
* Analyzes trends and evaluates the impact of changes in Health Authority requirements for e-submissions, communicating these changes to the relevant areas within Eisai and driving the necessary changes to processes and procedures.
* Ensure the timely completion of all administrative tasks for this position, including but not limited to monthly reports, performance objective setting, performance reviews, and training, for self and staff.
Hands-On Submission Support
* Actively participates in submission planning and execution, including document compilation, publishing, and quality checks.
* Provide technical oversight and troubleshooting for eCTD submissions and related systems.
Operational Excellence
* Ensure consistent application of GSM global procedures and standards.
* Proactively monitors and assess process performance, identifying opportunities for continuous improvement.
Requirements
* Bachelor's degree in scientific or information technology field; advanced degree preferred
* 8+ years of pharmaceutical industry regulatory experience
* 5+ years of experience with submissions management, process development, standards development and compilation of electronic major submissions required
* Proficient with U.S. and EU submission requirements including but not limited to Emerging Markets
* Advance experience with the drug development process and eCTD regulatory submission standards
* Expert understanding of Project Management concepts and techniques
* Ability to apply SOPs regulations pertaining to electronic submissions
* Ability to lead cross-functional team, establish effective relationships with team members and work well in a cross functional team environment
* Advance experience creating timelines for the development and submission of drug filings to regulatory health authorities
* Excellent organizational skills to support multi-task and manage submission timelines in a fast-paced environment with changing priorities
* Well-organized with the ability to multi-task and work with minimal supervision
* Ability to manage change to support organization's effectiveness by implementing change
* Effectively communicates written and verbal communication skills
* Demonstrates strong analytical, problem solving and critical thinking skills with the ability to analyze problems, identify alternative solutions and implement recommendations for resolution.
* Certification is a plus (such as Regulatory Affairs Professional Society (RAPS)
Technical Skills Required
* Advance working knowledge of global regulatory submission standards, publishing software, software validation concepts, and regulatory publishing best practices
* Proficiency in eCTD publishing tools (e.g., Lorenz docu Bridge, Extedo eCTDmanager, or equivalent).
* Strong understanding of ICH guidelines, regional regulatory requirements, and data standards (e.g., CDISC).
* Extensive experience with Regulatory Information Management (RIM) systems and Document Management Systems (e.g., Veeva Vault, SharePoint, Documentum)
* PowerPoint, SharePoint, XML, Adobe Acrobat, ISI Toolbox and eData transfer systems
* Ability to troubleshoot technical issues related to electronic submissions and publishing.
We are open to remote-based, but the preference for this role is a hybrid work arrangement in Nutley, NJ with 3 days a week in office every week (Tuesday, Wednesday. Thursday).
Eisai Salary Transparency Language:
The annual base salary range for the Associate Director, Global Submission Management is from :$159,000-$208,700
Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.
Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.
Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit **********************************************************
Certain other benefits may be available for this position, please discuss any questions with your recruiter.
Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.
Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:
Right To Work
E-Verify Participation
Auto-ApplyAssociate Director, Complementary and Integrative Medicine
Associate director job in Baltimore, MD
Sun Life U.S. is one of the largest providers of employee and government benefits, helping approximately 50 million Americans access the care and coverage they need. Through employers, industry partners and government programs, Sun Life U.S. offers a portfolio of benefits and services, including dental, vision, disability, absence management, life, supplemental health, medical stop-loss insurance, and healthcare navigation. We have more than 6,400 employees and associates in our partner dental practices and operate nationwide.
Visit our website to discover how Sun Life is making life brighter for our customers, partners and communities.
Job Description:
Sun Life embraces a hybrid work model that balances in-office collaboration with the flexibility of virtual work. Internal candidates are not required to relocate near an office.
The opportunity: The Associate Director of Complementary and Integrative Medicine (CIM) provides expert medical consultation, strategic direction, and program leadership for all CIM-related activities involving PinnaleCare members. This role combines clinical expertise with strategic, operational, and research oversight to deliver whole-person, patient-centered care. The Associate Director will guide the design, growth, and integration of CIM programs that align with PinnacleCare's mission, ensuring quality, innovation, and value for members.
How you will contribute:
* Establish the overall vision, mission, and strategic goals for PinnacleCare's CIM program.
* Lead the development and implementation of a multi-year strategic plan to expand CIM services, identify innovative opportunities, and strengthen partnerships that enhance member value.
* Serve as PinnaleCare's subject matter expert on complementary and integrative medicine, providing direct clinical consultation and guidance to health advisors and internal teams.
* Collaborate with the Chief Medical Officer (CMO) and organizational leadership to expand and manage the CIM Medical Advisory Board and provider referral network.
* Oversee program operations, productivity, and budget performance to ensure sustainability and measurable impact.
* Develop strategies to advance the visibility and increase usage of CIM services across the organization.
* Collaborate with the Research and Medical Intelligence teams in developing evidence-based reports, literature reviews, and data summaries on CIM topics.
* Work with the Director of Research to identify qualified members of the CIM clinical community to produce high level research reports for internal and external distribution
* Maintain and enhance the CIM clinician and facility database to ensure it remains current, credible, and aligned with evidence-based practice standards.
* Participate in complex case reviews and facilitate referrals to qualified CIM clinicians and specialists within the network.
* Develop and deliver training and professional development programs on CIM approaches, modalities, and evidence-based practices for internal staff.
* Collaborate with Marketing and Communications to highlight CIM program value, outcomes, and innovations in internal and external publications.
* Represent the CIM program at internal meetings, external conferences, and industry events to build awareness and credibility.
* Support Membership Development and Relationship Management teams with CIM-related education, resources and client consultations.
* Provide operational oversight for all CIM activities to ensure high-quality member experience and alignment with PinnacleCare standards.
* Build and maintain relationship with CIM clinicians, vendors, and strategic partners to support service excellence and continuity of care.
* Identify and implement process improvements to enhance efficiency, member satisfaction, and cost effectiveness.
* Resolve clinical and operational issues related to CIM services and referrals in collaboration with internal and external partners.
What you will bring with you:
* Ability to work with a diverse range of people
* Doctor of Naturopathic Medicine (ND) degree from an accredited naturopathic medical college
* Board certification by the North American Board of Naturopathic Examiners
* Demonstrated experience in program leadership, strategic planning and service expansion within the field of integrative medicine
* Strong clinical foundation and working knowledge of Complementary, Alternative and Integrative modalities
* Excellent interpersonal, written and verbal communication skills with the ability to collaborate effectively across disciplines
* Proven ability to balance clinical quality with financial and operational priorities
* Proficiency with Microsoft office Suite
* Strong problem-solving, organizational and analytical skills
Salary:
$109,400-$164,100
At our company, we are committed to pay transparency and equity. The salary range for this role is competitive nationwide, and we strive to ensure that compensation is fair and equitable. Your actual base salary will be determined based on your unique skills, qualifications, experience, education, and geographic location. In addition to your base salary, this position is eligible for a discretionary annual incentive award based on your individual performance as well as the overall performance of the business. We are dedicated to creating a work environment where everyone is rewarded for their contributions.
Not ready to apply yet but want to stay in touch? Join our talent community to stay connected until the time is right for you!
We are committed to fostering an inclusive environment where all employees feel they belong, are supported and empowered to thrive. We are dedicated to building teams with varied experiences, backgrounds, perspectives and ideas that benefit our colleagues, clients, and the communities where we operate. We encourage applications from qualified individuals from all backgrounds.
Life is brighter when you work at Sun Life
At Sun Life, we prioritize your well-being with comprehensive benefits, including generous vacation and sick time, market-leading paid family, parental and adoption leave, medical coverage, company paid life and AD&D insurance, disability programs and a partially paid sabbatical program. Plan for your future with our 401(k) employer match, stock purchase options and an employer-funded retirement account. Enjoy a flexible, inclusive and collaborative work environment that supports career growth. We're proud to be recognized in our communities as a top employer. Proudly Great Place to Work Certified in Canada and the U.S., we've also been recognized as a "Top 10" employer by the Boston Globe's "Top Places to Work" for two years in a row. Visit our website to learn more about our benefits and recognition within our communities.
We will make reasonable accommodations to the known physical or mental limitations of otherwise-qualified individuals with disabilities or special disabled veterans, unless the accommodation would impose an undue hardship on the operation of our business. Please email ************************* to request an accommodation.
For applicants residing in California, please read our employee California Privacy Policy and Notice.
We do not require or administer lie detector tests as a condition of employment or continued employment.
Sun Life will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including applicable fair chance ordinances.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Job Category:
Medical Services
Posting End Date:
11/01/2026
Auto-ApplyChief Operating Officer
Associate director job in Baltimore, MD
About Our Client Our client is a rapidly expanding biotechnology company at the forefront of developing groundbreaking therapies for a range of rare diseases. Their mission is to translate cutting-edge scientific research into life-changing medical solutions. With a robust pipeline of clinical-stage assets and a commitment to patient-centric innovation, they are poised to become a leader in the precision medicine and pharmaceutical industries. The Opportunity Our client is seeking a visionary and results-driven Chief Operating Officer to lead all operational functions and spearhead the next phase of company growth. This pivotal role is focused on unifying the research and development, clinical operations, and commercialization teams under a single, cohesive go-to-market strategy. You will be responsible for defining and executing a comprehensive operational strategy to accelerate product development, navigate regulatory hurdles, and prepare for market launch.
You will be instrumental in driving sustainable operational growth, optimizing the entire product lifecycle, and building a high-performing, data-driven operational organization. This is a unique opportunity for a senior leader who thrives on building and scaling teams and wants to make a direct impact on the company's trajectory in a highly visible role. What You Will Do
Develop and execute a comprehensive operational strategy to achieve ambitious growth targets and expand market leadership.
Lead and mentor the research, clinical, and commercial teams, fostering a culture of accountability and high performance.
Drive the entire operational cycle, from early-stage research and clinical trial management to regulatory submissions and market commercialization.
Identify new market opportunities and strategic partnerships to diversify revenue streams.
Collaborate with executive leadership to align operational goals with overall business objectives and resource allocation.
Utilize data and analytics to forecast pipeline progress, measure performance, and optimize development and commercial effectiveness.
Act as a key external representative, engaging with top-tier partners and industry leaders to strengthen brand presence and close key deals.
Who You Are
A Strategic Leader: You have a proven ability to develop and execute multi-year operational strategies that drive significant top-line growth. You think holistically about the product development lifecycle and how different functions can align to create a seamless experience.
A Team Builder: You are skilled at recruiting, developing, and inspiring high-performing teams. You lead by example and empower your direct reports to achieve their full potential.
Results-Oriented: You have a verifiable track record of exceeding operational targets in a competitive B2B environment, with a strong focus on both new business acquisition and client expansion.
Ideal Candidate Profile We are seeking a Chief Operating Officer with extensive experience in the pharmaceuticals, biotechnology, or life sciences industries. Candidates with a successful history of leading and scaling operational teams in parallel sectors-such as medical devices, clinical diagnostics, or B2B software-will also be strongly considered. Why Join This Team? This is your chance to play a key role in a company that is at the forefront of the biotechnology industry. If you are a strategic leader who thrives on building and scaling operational organizations, you will have the opportunity to shape the future of the company and earn significant equity and commissions. You'll be part of a supportive executive team and backed by cutting-edge solutions that are in high demand across the globe. ________________________________________ About Naviga Recruiting & Executive Search Naviga Recruiting & Executive Search is a leading provider of Contingent Workforce Solutions, Executive Search, Leadership and Individual Contributor hiring, empowering businesses to achieve their strategic objectives through expert talent acquisition. Our specialties include sales, marketing, finance/accounting and operations hiring. With a commitment to excellence and a deep understanding of market trends, Naviga Recruiting & Executive Search helps organizations build high-performing teams and navigate complex workforce challenges. Naviga Recruiting & Executive Search specializes in U.S. Hiring for Global Businesses.
Chief Operating Officer
Associate director job in White Marsh, MD
Job Details 5812 ALLENDER RD - WHITE MARSH, MDDescription
Responsibilities of the COO:
1. Oversee Daily Operations
Manage the day-to-day operations of the company to ensure efficiency and effectiveness.
Oversee process and procedures across all departments.
2. Execute Strategic Initiatives
Optimize systems, processes, and workflows to reduce costs, improve quality, and scale sustainably.
Leads initiatives with IT implementations, process automation, and lean/six sigma improvements
Direct branch expansion strategies
Identify branch locations based on owners' strategic growth plan
Negotiate leases with landlords
Oversee set up of production facilities using 5S principles
Ensure consistent policies and procedures across all branches
3. Performance & KPI Management
Monitor key metrics associated with efficiency of operations and ensure Production, Safety, Customer Service, Transportation, Project management, A/R & A/P and Construction Service Departments are meeting their objectives.
Collaborate with direct reports to correct any divergencies from internal Operation-related KPI Goals.
Monitor and manage P&L performance
4. Team Leadership & Culture
Direct Reports include:
Dir. Of Construction Service
Regional Branch Managers
Safety Director
Director of Sales
Director of Marketing and Innovation
Director of Customer Service
Use data to identify areas for improvement.
Foster a company culture that encourages great customer service, positive attitudes, reliability and accountability, continuous learning of new skills and teamwork with co-workers.
5. Operational Budgeting & Cost Control
Work closely with the CFO to manage operational budgets.
Optimize processes to improve efficiency and reduce costs.
6. Process Improvement
Analyze internal processes and identify ways to improve them for better productivity, safety and scalability.
Lead continuous improvement initiatives.
7. Asset Management
Oversee production, procurement, inventory, and delivery processes.
Ensure quality control and timely fulfillment of products/services.
Create and implement asset protection policies and procedures for fleet inventory
8. Risk & Compliance Management
Ensure operational activities comply with local, state, and federal laws and regulations.
Help build risk management processes related to operations.
Manage audits (other than financial), certifications
Ensure that company is in compliance with insurance requirements
9. Internal & External Partnerships
Manage key vendor, supplier, and strategic partner relationships tied to operations. (Purchasing of trailer assets for lease to be done by CEO)
Negotiate contracts and agreements with vendors that support operational goals. (CEO will negotiate purchases with manufacturers.)
10. Reporting
Provide regular updates on operational performance and strategic execution to the CEO and Sr. Leadership team.
Communicate to CEO the need to purchase fleet inventory
Participate in Same Page meetings every other week with CEO.
Area Director - Maryland East
Associate director job in Maryland
Reporting to the Sr. Director, US Core, the role of Area Director (AD) is critical to the success of Members and Chapters of BNI . The AD is actively engaged in team building, training, education, goal setting and attainment, and leading the Area Team and ensuring business growth for members and the area. The AD sets the vision for the Area and develops a professional and positive culture.
Additionally, the AD focuses on ensuring that Members and Directors achieve their own business goals and have a positive impact on the community.
Roles and Responsibilities:
Develop and Lead the Support and Launch Teams within the Area
Actively identify, observe, and invite qualified candidates to learn more about the Ambassador and Director Programs. Support the interview process. Ensure that the candidates in the process are coachable, compatible, and complementary to you, as well as a good fit for the Area and Regional teams.
Ensure all Directors participate in and complete the required training or orientation within their first 60 days on the team.
Support each LDC to achieve their goal(s) efficiently and provide necessary resources.
Conduct a Weekly Success Call with Chapter Leaders. The goals of the Weekly Success Calls are to discuss progress of the chapters, training, and resources needed to ensure the Chapter leaders are provided with needed training and resources.
Handle all questions and challenges from Directors and Ambassadors in a timely manner.
Conduct Regional Team meetings. These meetings are focused on creating a strong team bond and provide the necessary education, coaching, and discussion of current topics.
ADs are responsible for regional growth and for managing the LDCs in their regions. Managing LDCs may include coordinating with the Regional Development Team or Regional Director to develop a market growth plan, help recruit LDCs, ensure LDCs are trained and supported to achieve their goals.
Support launch initiatives and activities.
Collaborate with and provide feedback with your Member Success Concierge to ensure processes are followed and effective to provide necessary first-year Member support, Member issues are resolved efficiently, assistance for growth and training initiatives is provided, and retention issues are addressed.
Increase and Retain Chapter Memberships to grow the Area
Ensure every Chapter in the area has a Goal Plan in place and support the plan by providing resources and training.
Understand the training needs of Chapters and provide appropriate training as needed.
Support the area in planning and executing socials, trainings, and growth events that are within budget.
Execute an annual Member/Chapter Recognition event and other recognition or national events as necessary.
Support new Chapters and provide additional first year support and training.
Conduct monthly Regional Team meetings. These meetings are focused on creating a strong team bond and provide the necessary education, coaching, and discussion of current topics. These meetings are non-mandatory for the Regional Team.
Prospect by attending other networking events and developing a regional pipeline.
Identify opportunities to improve retention and develop and execute a strategy to increase it.
Ensure Overall Area Success
Ensure goals are achieved through a growth strategy that is consistent with ethical business practices.
Develop and maintain a professional and positive culture in your area.
Participate in a Weekly Success Call with the Regional Director. The purpose of these calls is education, training, evaluation of progress of area goals, evaluation of progress on your business goals, and an opportunity to answer any questions concerning Chapters or processes that arise throughout the week.
Schedule, plan, and execute all required regional and area trainings and events.
Plan and execute Chapter Success Trainings in September and Goal Planning Sessions in January.
Schedule, plan and execute monthly Leadership Team Roundtables. The roundtables will focus on education, review of area reports, leadership activities, and sharing of best practices.
Analyze the respective summary reports and Traffic Lights reports in BNI Connect monthly, to assess needed support for all Chapters in your area. Use this information to support the Leadership Teams, Ambassadors, and Directors in raising the level of participation of all Members in the Chapters, assisting the Chapters, and their members to reach their goals, including Chapter growth and increasing Member retention.
Conduct an annual goal planning/strategic planning session with your Regional Director and Regional Development Manager. Communicate the region's goals during a Regional Team Meeting.
Engage with Member Relations Coordinator regularly to ensure Member issues are appropriately addressed, identify and develop internal and external training and process opportunities to reduce the number of issues in the area.
Work with the Operations team to ensure administrative and operational duties are handled in a timely and accurate manner.
Demonstrated Competencies:
Communication - The capacity to convey information, ideas, and emotions in a clear, professional, and engaging manner across different contexts, audiences, and mediums. Focuses include listening actively, adapting tone and style, and understanding the social and emotional dynamics involved.
Leadership - Guiding and motivating others, performance management, setting clear expectations, and fostering a positive work environment. Making sound decisions and developing buy-in through trust and vision.
Creativity/Innovation - The capacity to think outside the box and generate innovative ideas. Adapting to change and engaging in continuous learning and critical thinking to promote the growth of the individual and the organization.
Conflict Resolution - The ability to identify, address, and manage conflicts constructively. This often involves fostering collaboration, communication, problem-solving, and emotional intelligence.
Customer Service - Ability to effectively support and engage with customers to meet their needs, resolve issues, and foster positive relationships. Focuses on blending interpersonal, problem-solving, and communication skills that drive customer satisfaction and loyalty.
Relationship Building - “Building strong relationships creates an environment of trust and support that yields happiness, opportunity, and meaning “. The ability to establish and maintain positive and effective working relationships.
Business Acumen - Ability to understand and apply business principles and concepts to make effective decisions and drive organization success, essentially how a business operates, makes money, and how individuals within that business contribute to its overall success.
Initiative - The ability to assess and initiate things independently. Takes proactive action, drives progress without needing constant direction, self-motivated. Has resourcefulness and a willingness to go beyond assigned tasks.
Accountability & Integrity - “We keep the promises we make, especially when it is hard to do so. This creates trust and supports strong relationships.” Taking responsibility for one's actions and outcomes, ensuring commitments are met, and learning from mistakes. Honest and having strong moral principles. .
Performance Management -Ability to effectively oversee, evaluate, and enhance employee performance to align with organization goals. Setting expectations, providing feedback, and fostering continuous improvement.
Required Qualifications:
Proven experience in a people manager position
Experience in developing profitable strategies and implementing vision
Strong understanding of performance management principles
Familiarity with diverse business functions such as marketing and budgeting.
Self-starter with outstanding organizational and leadership skills
Analytical abilities and problem-solving skills
Ability to provide constructive feedback and coach each team member to reach their full potential
Excellent communication and public speaking skills
Any additional duties needed to help demonstrate our core values, drive our vision, and fulfill our mission.
Preferred Qualifications:
BNI Director for at least 1 year
Demonstrated success launching BNI Chapters
Physical Demands and Working Conditions:
Sedentary work. Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects. Repetitive motion. Substantial movements (motions) of the wrists, hands, and/or fingers. The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading.
This is a full-time position. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
An equal opportunity employer.
Auto-ApplyAssociate Director of Academic Advising, College of Engineering [R0148937]
Associate director job in Maryland
The University of Nevada, Las Vegas (UNLV) appreciates your interest in employment. We ask that you keep in mind the following when completing your application:
Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process.
Required attachments are listed below on the posting. Your application will not be considered without the required attachments.
Please note that applications must be submitted prior to the close of the recruitment.
Once a recruitment has closed, applications will no longer be accepted. If you need assistance or have questions regarding the application process, please contact Human Resources at ************** or *****************
Job Description
The University of Nevada, Las Vegas invites applications for Associate Director of Academic Advising, College of Engineering [R0148937].
ROLE of the POSITION
This position, along with the Director of the Advising Center, academic advisors and an administrative assistant, is responsible for staffing the College of Engineering Advising Center. The purpose of this position is to help achieve the Center's goals of advising students, retaining existing students, assist with campus and college orientation events, tracking current students and graduates, and other assigned duties as designated by the Director.
The Associate Director will be tasked with managing the RPC objectives within the College of Engineering Advising Center. The Associate Director will be responsible for serving as the liaison to the greater UNLV community related to RPC initiatives, and will oversee RPC initiatives within with the College of Engineering. Specifically, the Associate Director will be responsible for coordination of early outreach and will manage advising of the students on academic warning and suspension. This position will work with the first-year student liaison and Director of Student Success for the development, maintenance and expansion of group advising beyond new student orientation to encompass group advising for all first-year students and second-year students with a focus on sophomore retention efforts.
The Associate Director will assist the Director in the training of advisors on RPC-related policies as it relates to academic advising. The Associate Director will advise a caseload of undergraduate students within the College - the Associate Director will specifically advise students on academic warning with the college and students being placed onto suspension/returning from suspension.
Extensive knowledge of the general education degree requirements for all College of Engineering majors offered at the university is essential for this position. Advisors use their experience in advising to assist students with identifying their strengths, interests, and abilities and interpret how these aspects of personality relate to majors and careers in order to progress through the major selection process.
This is a student facing service-based position. Additional duties will include, but are not limited to: review and articulate transfer coursework, advise and evaluate student's degree progress, interpret and correct degree audits, help at-risk students develop remedial plans of study and refer to appropriate campus services, help students process forms, serve as an advocate for students through communication with appropriate Faculty Senate committees, maintain detailed advising records utilizing a variety of software programs, assist with college and university recruiting, New Student Orientation and service events.
This position requires occasional evening and weekend responsibilities.
MINIMUM QUALIFICATIONS
This position requires a Master's Degree from an accredited college or university as recognized by the United States Department of Education and/or the Council on Higher Education Accreditation (CHEA) and 3 to 5 years of related professional, and minimum 1 year supervisory experience . Credentials must be obtained prior to the employment start date.
PREFERRED QUALIFICATIONS
Experience working with students on academic warning or suspension. Basic evaluation, assessment, data management, and reporting skills. Solid working knowledge of software programs such as MyUNLV (PeopleSoft), SalesForce, Google Docs, Microsoft Word, Excel, and PowerPoint is also desired.
COMMITMENT to DIVERSITY and CAMPUS VALUES
A successful candidate will support diversity, equity, and inclusiveness and contribute to a respectful, positive work environment. They will use our Campus Values to guide their decisions and actions and demonstrate our Rebel spirit.
SALARY
Salary competitive with those at similarly situated institutions.
BENEFITS OF WORKING AT UNLV
Competitive total rewards package including:
Paid time off, sick leave, and holidays
Excellent health insurance including medical, dental and vision
Comprehensive retirement plans and voluntary benefits programs
No state income tax
Tuition discounts at Nevada System of Higher Education (NSHE) schools
Tuition discounts for spouses, domestic partners, and dependents
PERKS & PROGRAMS
Employee recognition and appreciation programs
UNLV athletics ticket discounts
Statewide employee purchase program discounts
RebelCard discounts on and off campus
Wellness programming for all UNLV faculty and staff at no cost
Opportunity for career advancements to leadership roles
Connect with colleagues with shared interests
Personal and professional development opportunities
A comprehensive onboarding program, Rebels: Onboard
Support and resources available for veteran applicants - contact ********************** or visit our Veterans Webpage.
HOW TO APPLY
Submit a letter of interest, a detailed resume listing qualifications and experience, and the names, addresses, and telephone numbers of at least three professional references who may be contacted. References will not be contacted until the search chair notifies you in advance.
Applicants should fully describe their qualifications and experience, with specific reference to each of the minimum and preferred qualifications because this is the information on which the initial review of materials will be based.Materials should be addressed to Christopher Parker, Search Committee Chair.
Although this position will remain open until filled, review of candidates' materials will begin on October 27, 2025.
Applications must be submitted electronically through Workday. Please note that emailed materials will not be accepted.
Veterans are encouraged to apply. UNLV values the skills of those who have served. Learn more at Veterans Webpage or contact ********************** for support.
For assistance with the application process, please review instructions on How to Apply. For further assistance contact UNLV Human Resources at ************** or *****************.
SPECIAL INSTRUCTIONS FOR INTERNAL NSHE CANDIDATES
UNLV employees or employees within the Nevada System of Higher Education (NSHE) MUST use the “Find Jobs” process within Workday to find and apply for jobs at UNLV and other NSHE Institutions. Once you log into Workday, type "Find Jobs" in the search box which will navigate to the internal job posting site. Locate this specific job posting by typing the job requisition number, “R0148937” in the search box.
If you complete an application outside of the internal application process, your application will be returned and you will have to reapply as an internal applicant which may delay your application.
PROFILE of the UNIVERSITY
Founded in 1957, UNLV is a doctoral-degree-granting institution comprised of approximately 30,000 students and more than 3,600 faculty and staff. To date, UNLV has conferred more than 152,000 degrees, producing more than 130,000 alumni around the world. UNLV is classified by the Carnegie Foundation for the Advancement of Teaching as an R1 research university with very high research activity, and is a recipient of the Carnegie Classification for Community Engagement. The university is committed to recruiting and retaining top students and faculty, educating the region's diversifying population and workforce, driving economic activity through increased research and community partnerships, and creating an academic health center for Southern Nevada that includes the launch of a new UNLV School of Medicine. UNLV is located on a 332-acre main campus and two satellite campuses in Southern Nevada.
Here at UNLV, we have come together and created one of the most affirmative and dynamic academic environments in the country. UNLV sits in the top spot in U.S. News & World Report's annual listing of the nation's most diverse universities for undergraduates. The university has ranked in the top ten since the rankings debuted more than a decade ago. We continue to show our commitment to serving our wonderfully diverse population and building the future for Las Vegas and Nevada.
For more information, visit us on line at: *******************
EEO/AA STATEMENT
The University of Nevada - Las Vegas (UNLV) is committed to providing a place of work and learning free of discrimination on the basis of a person's age (40 or older), disability, whether actual or perceived by others (including service-connected disabilities), gender (including pregnancy related conditions), military status or military obligations, sexual orientation, gender identity or expression, genetic information, national origin, race (including hair texture and protected hairstyles such as natural hairstyles, afros, bantu knots, curls, braids, locks and twists), color, or religion (protected classes). Discrimination on the basis of a protected class, including unlawful harassment, which is a form of discrimination, is illegal under federal and state law. Where unlawful discrimination is found to have occurred, UNLV will act to stop the unlawful discrimination, to prevent its recurrence, to remedy its effects, and to discipline those responsible. Women, minorities, and veterans are encouraged to apply.
TITLE IX STATEMENT
The University of Nevada, Las Vegas, does not discriminate on the basis of sex in any education program or activity that it operates. Non-discrimination on the basis of sex is mandated by Title IX of the Education Amendments of 1972 (20 U.S.C. §§ 1681 et seq.) and the corresponding implementation regulations (34 C.F.R. Part 106). The University's commitment to nondiscrimination in its education programs and activities extends to applicants for admission and employment. Inquiries concerning the application of these provisions may be referred to: Michelle Sposito, J.D., Title IX Coordinator, University of Nevada, Las Vegas, 4505 S. Maryland Parkway, Mail Stop 1062, Las Vegas, NV 89154-1062, Campus Services Building (CSB) Room 246, Telephone: **************; Email: ***************************, or to The Assistant Secretary of the United States Department of Education, U.S. Department of Education, Office for Civil Rights, 400 Maryland Avenue, SW, Washington, D.C. 20202-1100; Telephone: ************** FAX: ************; TDD: **************; Email: **********; or to both.
Information pertaining to the University's grievance procedures and grievance process, including how to report or file a complaint of sex discrimination, how to report or file a formal complaint of sexual harassment, and how the University will respond can be found online at the Office of Equal Employment & Title IX webpage.
SAFETY AND SECURITY STATEMENT
UNLV is committed to assisting all members of the UNLV community in providing for their own safety and security. The Annual Security Report and Annual Fire Safety Report compliance document is available online.
JOB CATEGORY
Administrative Faculty
Yes
Full-Time Equivalent
100.0%
Required Attachment(s)
Submit a letter of interest, a detailed resume listing qualifications and experience, and the names, addresses, and telephone numbers of at least three professional references who may be contacted. References will not be contacted until the search chair notifies you in advance.
Posting Close Date
Note to Applicant
This position may require that a criminal background check be conducted on the candidate(s) selected for hire.
HR will attempt to verify academic credentials upon receipt of hiring documents. If the academic credentials cannot be verified, HR will notify the faculty member that an official transcript of their highest degree must be submitted within thirty days of the faculty member's first day of employment.
References will be contacted at the appropriate phase of the recruitment process.
As part of the hiring process, applicants for positions in the Nevada System of Higher Education may be required to demonstrate the ability to perform job-related tasks.
For positions that require driving, evidence of a valid driver's license will be required at the time of employment and as a condition of continued employment.
All document(s) must be received on or before the closing date of the job announcements (if a closing date is provided).
Recruitments that provide a work schedule are subject to change based on organizational needs.
Auto-ApplyDeputy Director Aerospace, Defense, and Critical Infrastructure Segment Owner
Associate director job in California, MD
About GlobalFoundries: GlobalFoundries is a leading full-service semiconductor foundry providing a unique combination of design, development, and fabrication services to some of the world's most inspired technology companies. With a global manufacturing footprint spanning three continents, GlobalFoundries makes possible the technologies and systems that transform industries and give customers the power to shape their markets. For more information, visit ***********
Summary of Role:
Reporting to the Senior Director of the ADCI End Market at GlobalFoundries, the Deputy Director Aerospace, Defense, and Critical Infrastructure (ASIC/SoC) Segment Owner will have subject matter expertise in microelectronics, including partnering with U.S. Government agencies, and will own defining and executing the strategy for business growth in this market segment. The Aerospace, Defense, and Critical Infrastructure Business targets commercial aerospace, national security, and critical infrastructure applications, including addressing regional supply requirements. This Segment role focus on analog and power applications, amongst others. Evolving requirements and standards require deep domain and thought leadership for GF to develop winning platforms for these markets. This position will provide thought leadership for GF engagements with customers spanning commercial, defense, and government entities. This leader will be responsible for the growth and program wins for this market segment and will develop and implement strategies that will successfully promote the organization's mission and meet its financial objectives.
Essential responsibilities:
* Understand market dynamics and requirements for Aerospace, Defense, and Critical Infrastructure, including land, air, sea, and space applications.
* Develop customer engagements in partnership with the GlobalFoundries Sales organization to understand customer's products, product roadmaps and corresponding technology needs.
* Identify the GlobalFoundries solution including technology platform, differentiating feature(s) and design IP that best serves a customer's needs and drives adoption.
* Build, maintain, and strengthen external relationships including customers & other external government authorities.
* Define the market requirements for new technology features and design IP to be developed in accordance with market needs. Identifies and shapes external partnerships to expand business line.
* Create Market Requirements Documents to inform GlobalFoundries product offerings
* Drive ownership and accountability in responsible organizations such as Sales, Design Enablement, Manufacturing Fab and Supply Chain to deliver to market needs.
* Drive opportunity funnel to growth targets, by working closely with customers to identify needs, GF solutions, and customer opportunities, entered into GlobalFoundries' opportunity management system and drive sales team pursuit to win.
* Create and deploy compelling presentation collateral to articulate the value of GF's solutions to the customer and end-users to drive adoption.
* Be a GlobalFoundries champion in all venues.
* Drive design win targets and create detailed plans to achieve them.
* Create a sense of urgency and drive clarity across multi-functional teams to achieve business objectives. Identify issues and address them head-on using data to move complex multi-site programs forward.
* Develop strategic relationships with customers and eco-system partners to achieve success across a 5+ year horizon.
* Serve as a champion of GlobalFoundries technology solutions with strong external presence at technology conferences, trade shows, webinars etc.
Other Responsibilities:
* Accountable for and drives commitment; to compliance with all internal policies and legal regulations in every area of the organizations daily activity, including development of short and long-term plans, policies, and guidelines
* Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety & Security requirements and programs
* Work and collaborate other projects and/or assignments as needed.
Required Qualifications:
* Bachelor's degree in Electrical Engineering or related field
* 7+ Years of Experience in either aerospace or defense at a product company, defense prime, or similar.
* Knowledge of working with U.S. Government agencies and related funding.
* The individual will need to possess broad technical and business skills to be successful in the role
* Semiconductor product experience
* ASIC and/or SoC experience with preference for mixed signal and analog. Digital ASIC and/or SoC experience also accepted
* Travel Requirements: 25% of travel
* Applicant must be a U.S. citizen.
* Must be eligible to obtain and maintain a SECRET level U.S. Government security clearance.
Preferred Qualifications:
* Master's Degree in Electrical Engineering or related field
* Deep domain expertise in microelectronics including for analog and power applications
* Deep domain expertise in aerospace and defense applications
Expected Salary Range
$131,900.00 - $241,500.00
The exact Salary will be determined based on qualifications, experience and location.
The role you are applying for may require you to obtain a US Department of Defense Security Clearance at some time during your employment. Acceptance of this role commits to applying for such if requested. Further, the applicant consents to being asked questions about their citizenship and background to assess the likelihood of obtaining a Security Clearance. The applicant also acknowledges that GlobalFoundries can only nominate and submit an application for a Security Clearance. The granting of a Security Clearance is at the sole discretion of the U.S. Government and the Department of Defense.
If you need a reasonable accommodation for any part of the employment process, please contact us by email at usaccommodations@gf.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
An offer with GlobalFoundries is conditioned upon the successful completion of pre-employment conditions, as applicable, and subject to applicable laws and regulations.
GlobalFoundries is fully committed to equal opportunity in the workplace and believes that cultural diversity within the company enhances its business potential. GlobalFoundries goal of excellence in business necessitates the attraction and retention of highly qualified people. Artificial barriers and stereotypic biases detract from this objective and may be illegally discriminatory.
All policies and processes which pertain to employees including recruitment, selection, training, utilization, promotion, compensation, benefits, extracurricular programs, and termination are created and implemented without regard to age, ethnicity, ancestry, color, marital status, medical condition, mental or physical disability, national origin, race, religion, political and/or third-party affiliation, sex, sexual orientation, gender identity or expression, veteran status, or any other characteristic or category specified by local, state or federal law
Auto-ApplyDirector, Wireless Services
Associate director job in Columbia, MD
If being a part of a world-class organization that operates in some of the most advanced technology environments around the world sounds like a dream job, Network Connex might be the right fit for you! You'll be part of a team working together to solve customer problems every day, with compensation and benefits that are an investment in your career, financial future, and overall well-being.
The Director of Wireless Services will supervise a wide range of programs responsible for the delivery and overall success of each program. You will supervise managers and inform management on progress and performance. The Director must have a broad knowledge of project and program management principles in the wireless industry, they must have a strategic mindset with entrepreneurial spirit, as well as be able to lead and develop their teams. The Director's goal is to ensure every project and program will be delivered successfully to the highest possible quality of the organization along with business growth.
Job Duties and Responsibilities:
Initiate and set goals for programs according to the strategic objectives of the organization.
Plan the programs from start to completion involving deadlines, milestones, and processes.
Develop or approve budgets and operations.
Build a book to bill business in the market with business contacts.
Devise evaluation strategies to monitor performance and determine the need for improvements.
Supervise all program and project managers involved to provide feedback and resolve complex problems.
Discover ways to enhance efficiency and productivity of procedures and people.
Apply change, risk and resource management principles when needed.
Evaluate reports from managers to monitor progress and flag potential issues.
Ensure program operations and activities adhere to legal guidelines and internal policies.
Keep senior management informed with detailed and accurate reports or presentations.
Job Knowledge, Skills, and Abilities:
Proven experience as Program Director or other managerial position.
Extensive (10+ years) experience within the telecommunications industry.
Demonstrated business development acumen to drive a minimum of 10% annual growth.
Background in site acquisition, wireless site development, DAS, Small cell and Macro site engineering services.
Thorough understanding of project/program management techniques and methods.
Excellent Knowledge of performance evaluation techniques and key metrics.
Outstanding knowledge of data analysis, reporting and budgeting.
Working knowledge of MS office and program management software.
A business acumen with a strategic ability.
Excellent organizational and leadership skills.
An analytical mindset with great problem-solving abilities.
Excellent communication skills.
Education and Experience:
Bachelor's or master's degree in Business, Engineering, Construction Management, or related field.
Physical Requirements:
Prolonged periods sitting at a desk and working on a computer.
Must be able to lift up to 15 pounds at times.
In addition to competitive base pay, Network Connex offers a comprehensive benefits package designed to support your physical, mental, and financial health and you can begin participating in our programs on the first of the month following your start date.
Join our Vanguard 401(k) plan, with immediate vesting and a generous company match to help you build long-term financial security. Our team also enjoys 10 paid company holidays, a generous PTO accrual schedule, and access to discounts on useful products and services.
EEOC-Minority/Female/Disability/Veteran
Network Connex believes all persons are entitled to equal employment opportunities and does not discriminate against employees or job applicants because of race, color, gender, affectional or sexual orientation, domestic partnership status, ancestry, religion, national origin, citizenship status, marital status, disability, veteran status, age or any other protected group status. Upon acceptance of an offer, all candidates will be required to pass a background check and drug screening.
Auto-ApplyVP of Branch Operations
Associate director job in Rockville, MD
Requirements
A day in the life of a VP of Branch Operations will include:
Promoting a sales culture and ensures that staff receive proper training and coaching to demonstrate abilities to sell/cross-selling products based on member needs
Leading and motivating a group of branches to attain or exceed branch loan, deposit, and revenue goals
Coaching and mentoring branch managers and staff on career development and sales process.
Creating and foster a culture of exceptional member service and sales
Being responsible for final approval of hiring, escalated progressive discipline, performance evaluation approvals, and performance development of staff. Conducts interviews, screening processes, hiring and performance management of Branch Managers and their staff as needed
Assisting managers in resolving complex member complaints
Monitoring the branch operating results relative to the goals that have been established by the executive team. Develops individual and team goals to reach branch goals
Assisting in directing the planning, recommending, and implementing programs and policies within the branches.
Monitoring branch activity, including tellers - number of transactions, volume, teller errors, cash ordering and ATM balancing, full vault security and balancing.
Working with the PVP of Business Development to develop operational procedures to maximize efficiency and quality of work to provide consistent quality service to members.
Holding periodic staff meetings to discuss areas needing improvement, changes in procedures, new developments, or services and to present general information.
Managing sales, service, and operational results by analyzing, planning, organizing, budgeting, monitoring/controlling, problem solving, decision making and managing change. Deliver reports in a timely and accurate manner.
Some travel required (branches)
Experience:
Ten years or more of similar or related experience to include seven years in financial institution/banking in a management role
Education:
A two- year college degree or completion of specialized certification/training
Corresponding experience
Top benefits or perks:
Joining Lafayette Federal comes with perks to support you in your personal and professional journey.
We provide employees with a generous benefits package including:
Employer paid (99.9%) health insurance premium for single and family coverage (HMO Plan)
Fully funded deductible (HMO Plan)
401k employer matching contribution
Income protection with life insurance, short and long-term disability
Paid time off, holiday leave & birthday leave
Educational assistance
Commuter benefits program and more!
The job posting highlights the most critical responsibilities and requirements of the job. It is not all-inclusive. There may be additional duties, responsibilities, and qualifications for this job.
Pay: $111,935 - $125,000 annually depending on experience and qualifications.
*Lafayette Federal Credit Union is an Equal Opportunity and E-Verify Employer
*EOE/AA/DISABILITY/VETERAN
Associate Director of Counseling Services - McDaniel College
Associate director job in Westminster, MD
In collaboration with the Assistant Dean of Student Health and Wellness, the Associate Director of Counseling Services provides leadership, clinical expertise, and operational oversight to the delivery of high-quality, culturally responsive, and evidence-based mental health services. The Associate Director utilizes a data-driven approach to ensure that clinical services are delivered effectively, ethically, and in alignment with departmental policies and procedures. This role oversees the day-to-day clinical operations of Counseling Services including staff scheduling, case management processes, and clinical coverage. The Associate Director maintains a reduced but consistent caseload, providing direct clinical services to model best practices and support service delivery, and serves as a key resource in crisis intervention and staff consultation.
Specific Duties and Responsibilities
* Manages the day-to-day clinical operations of Counseling Services to ensure the delivery of high-quality mental health services and ensures adequate clinical coverage.
* Collaborates with the Assistant Dean to develop, enforce, review, and update policies and procedures for Counseling Services to enhance the overall effectiveness and efficiency of service delivery.
* Functions as a super user and system administrator for Titanium, the Electronic Health Record (EHR). Assists staff in troubleshooting issues that arise during utilization, creates and maintains clinical forms and templates within Titanium, and performs regular chart auditing to ensure staff complete accurate and timely clinical documentation in accordance with state and federal law, professional ethics, and Wellness Center policies.
* Coordinates the Wellness Extended Support Program, a fee-based program that offers students long-term individual counseling and clinical case management.
* Coordinates the planning and implementation of group therapy offerings each semester.
* Orients and trains new counseling staff and trainees in their clinical job responsibilities.
* Assists in providing staff support and direction, promoting accountability, enforcing deadlines, and providing feedback related to ongoing performance to all counseling team members as needed to maintain operational excellence.
* Provides clinical supervision for counseling services staff, specifically the hours of clinical supervision required for early-career clinicians before they achieve independent licensure.
* Assists in the supervision of administrative support staff to ensure the effective execution of front desk procedures/protocol, manage workflow, and provide support in serving distressed clients and managing clinical emergencies.
* Provides just-in-time clinical consultation to counseling staff and trainees as needed, particularly related to crisis situations, policy interpretation, and emergent complex cases. Determines when it is necessary to involve the Assistant Dean in decision making.
* Coordinates clinical risk management processes, including crisis intervention, hospitalization, and referral to higher levels of care while keeping the Assistant Dean and other authorized stakeholders informed.
* Co-facilitates the weekly Clinical Consultation and Disposition meeting in which the Counseling Services team reviews treatment planning for high acuity, challenging, and/or shared cases to ensure quality of service delivery and engages in peer consultation and support.
* Coordinates, schedules, and facilitates the series of Culturally Responsive Case Conferences in which each clinical staff member and trainee present at least once each academic year to support continued professional development.
* Assists in providing and/or organizing training sessions and professional development opportunities to promote collegiality, optimum and ethical performance, and teamwork.
* Collaborates with the clinical and administrative support staff to update/maintain forms, documents, brochures, fliers, and marketing strategies related to Counseling Services.
* In collaboration with the Assistant Dean, ensures all staff are kept abreast of the legal and ethical guidelines pertaining to the delivery of clinical services and documentation.
* Identifies and implements strategies to ensure that counseling services and programs meet the needs of McDaniel's diverse student population.
* Coordinates a comprehensive clinical training program for graduate students in various mental health fields. This includes trainee selection, training, clinical supervision, evaluation, and affiliation responsibilities as well as oversight of other clinical staff providing supervision to trainees.
* Develops and implements consistent quality assurance practices and operational metrics for counseling services.
* Partners with the Assistant Dean in utilizing a data-driven approach of evaluating counseling services through data collection, service utilization tracking, and outcome measures. Identify system issues, anticipate the cost/benefits, risks, and organizational impact of decisions, and implement effective solutions in clinical operations, policies, and procedures.
* Contributes to short- and long-range strategic planning for Counseling Services that aligns with the mission, vision, and goals of the Wellness Center, the division of Academic and Campus Life, and McDaniel College.
* Remains current in evolving evidence-based and outcomes-driven best practices for a college-based mental health care setting through involvement in appropriate professional organizations and ongoing professional development.
* Contributes to the division of Academic and Campus Life and college by attending and/or supporting events, activities, and programs sponsored by areas outside of the Wellness Center (e.g., campus-wide traditions, events, programs, etc.)
* Act as the Assistant Dean's designee in their absence for operational and clinical matters.
Essential Duties and Responsibilities for all Mental Health Counseling Staff
* Provides intake assessments and effective treatment planning.
* Provides individual and group counseling to students presenting with a variety of personal, social, academic, and mental health concerns.
* Provides case management and appropriate referrals to off-campus providers as needed.
* Provides crisis assessment, intervention, and consultation as needed during working hours and on-call rotation for evenings and weekends.
* Seeks immediate consultation with the Assistant Dean in situations where there is imminent concern for a student's safety or the safety of others.
* Provides professional consultation to faculty, staff, college administrators, and family members of students as needed.
* Establishes and maintains collaborative relationships with local hospitals, substance abuse and mental health agencies, and mental health professionals.
* Maintains accurate, adequate, and timely documentation of treatment records including assessment, treatment plans, progress notes, correspondence with others, and termination records.
* Follows professional ethics, state laws, FERPA, and McDaniel College Wellness Center procedures for the administration and documentation of treatment records.
* Collaborates with other departments across campus (Residence Life, Student Engagement, Student Belonging, Student Accessibility and Support Services, Academic Life, etc.) to further develop the holistic well-being of all students.
* Maintains professional licensure and credentials in good standing including the completion of required continuing education credits.
* Observes state and national statues and guidelines related to professional role, code of ethics, and confidentiality including FERPA.
* Attends weekly Clinical Consultation and Disposition meetings, biweekly Counseling staff meetings and Wellness Center staff meetings, departmental and divisional professional development sessions, and other meetings assigned by the supervisor.
* Contributes to the Wellness Center's outreach programming including skill-based workshops and prevention and educational programs, including those that are part of orientation activities and other college-wide programs and events.
* Generates up-to-date and accurate reports as needed.
* Serves as a member of campus committees as assigned.
* Performs other duties as assigned.
Information Security Role: Data User
* Follow the policies and procedures established by the appropriate Data Stewards.
* Comply with federal and state laws and regulations as well as College policies, procedures, and standards associated with the College computing resources and institutional data used.
* Use institutional data only as required for the conduct of College business within the scope of employment.
* Implement safeguards prescribed by appropriate Data Stewards for Limited Access and Restricted Data.
* Ensure the appropriateness, accuracy, and timeliness of institutional data used for the conduct of College business.
* Report any unauthorized access, data misuse, or data quality issues to the appropriate Data Steward for remediation.
* Accept and complete the confidentiality statement yearly if access includes Restricted data.
* Report any suspected data breach to the CIO and the IT Help Desk as soon as possible.
Requirements:
Minimum Qualifications
* Master's degree in social work, mental health counseling or related field
* Independently licensed to practice in the state of Maryland as clinical social worker (LCSW-C), professional counselor (LCPC), or licensed psychologist.
* Minimum of 3 years of post-licensure clinical experience.
* Demonstrated expertise in crisis response, risk assessment, and evidence-based treatment.
* Demonstrated ability to work collaboratively with a multidisciplinary team of mental health clinicians.
* Experience providing culturally responsive treatment to a diverse client population.
* Demonstrated skill in working well under pressure to prioritize and manage multiple clinical responsibilities.
* Excellent verbal and written communication skills.
* Successful completion of a background and credential background check
* Experience working with Microsoft Office applications (e.g. Word, Excel, PowerPoint), electronic health records.
* Ability to participate in on-call coverage rotation and emergency response.
Working Conditions
* While performing the duties of this job, the employee is routinely working in a normal office environment with minimal exposure to adverse conditions. The noise level in the work environment is usually minimal.
Physical Abilities
The physical demands described below are representative of those that must be met by an employee to successfully perform the essential functions of this job:
* Sitting for long periods of time.
* Some bending and stooping when working with files.
* Limited lifting involved but not more than 10 pounds at a time.
Additional Information:
McDaniel College, in compliance with federal and state laws and regulations, does not discriminate in the recruitment, admission, and employment of students, faculty, and staff in the operation of any of its educational programs and activities. McDaniel College will not tolerate any discrimination or harassment on basis of any protected status including protective hairstyle, race, religion, color, ancestry or national origin, disability, age, sex, gender, gender identity, gender expression, sexual orientation, pregnancy, military status, genetic information, marital status, veteran's status, or any other actual or perceived legally protected characteristics.
Application Instructions:
Completed applications must include the following: cover letter addressing position qualifications and related experience, resume, portfolio, names and contact Information of three professional references, a completed job application. Review of applications begins immediately. The position will remain open until filled.
Please click the Apply Now button below to begin your application.
Associate Director, Global Product Quality - GMP Processes
Associate director job in Annapolis, MD
The Associate Director, Global Product Quality - GMP Process is responsible for enabling the optimization and harmonization of key GMP quality practices across the global organization. This role defines, maintains continuously improves critical quality system elements including **Product Quality Complaints (PQC), Corrective and Preventive Actions (CAPA), Deviations, and Change Control** , ensuring compliance with global regulatory requirements and internal standards. The successful candidate will lead cross-functional initiatives to enhance quality performance, reduce risk, and foster a culture of continuous improvement.
**Key Responsibilities**
+ Process Ownership & Governance:Lead the global strategy and governance for Product Quality Complaints, CAPA, Deviations, and Change Control processes. Develop and implement global standards, procedures, and best practices to ensure consistency and compliance across all global affiliates. Partner with regional and site quality leaders to drive process improvements, enhance efficiency, and ensure alignment with corporate quality objectives
+ Cross-functional Leadership:Collaborate with Regulatory Affairs, Technical Operations, Manufacturing, and Supply Chain to ensure alignment and integration of quality into product lifecycle activities.
+ Quality Strategy Development:Lead or support global projects related to digital transformation, system upgrades, and process optimization.
+ Inspection Readiness & Compliance:Support regulatory inspections and internal audits, ensuring readiness and robust documentation of quality system performance.
+ Metrics and Reporting:
Monitor and report on key performance indicators (KPIs) to senior leadership, identifying opportunities for improvement and risk mitigation.
+ Training & Change Management:Provide leadership, coaching, and subject matter expertise to global teams on GMP compliance and quality system execution.
**Qualifications**
Required
+ Bachelor's degree in Pharmacy, Chemistry, Biology, Engineering, or related field (Master's or PhD preferred).
+ 8+ years of experience in pharmaceutical quality, regulatory affairs, or technical operations.
+ Proven expertise in managing and optimizing PQC, CAPA, deviation, and change control systems.
+ Experience leading cross-functional teams and global projects.
+ Skills & Competencies:
+ Strong knowledge of GMP, ICH guidelines, and global regulatory requirements.
+ Strong analytical skills with experience in quality metrics, risk management, and root cause analysis.
+ Excellent project management, communication, and stakeholder engagement skills.
+ Strategic thinker with a continuous improvement mindset.
+ Proficiency in quality systems and digital tools (e.g., TrackWise, Veeva).
Preferred Experience:
+ Certification in Lean, Six Sigma, or Quality Auditing.
+ Experience in global matrix organizations and cross-cultural collaboration.
+ Knowledge of digital transformation in quality processes
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $146,955.00 - Maximum $219,650.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Associate Director, Global Submission Management
Associate director job in Bethesda, MD
At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.
The Associate Director of Global Submission Management (GSM) is responsible for leading, managing, strategizing, and overseeing the planning, preparation, coordination, and delivery of global regulatory submissions in compliance with applicable regulations and standards. This role involves providing hands-on operational support for submission activities while ensuring strategic alignment and process optimization across different regions. It also includes resource planning, budgeting, vendor management, and technical oversight to support the objectives of Global Regulatory Operations. The Associate Director will collaborate with the Heads of Submissions Management for the EU and Japan as needed and utilize "Follow-the-sun" processes to ensure submission timelines are met regardless of the region.
The Associate Director, Global Submission Management (GSM, is responsible for the effective operation of Global Submission projects, ensuring the consistent application of global procedures and standards, and proactively assessing process performance for necessary optimizations. The Associate Director serves as the primary liaison between R&D functions, acting as the submission lead for designated global applications (e.g., INDs, NDAs, MAAs, supplements, amendments, and variations), to facilitate cross-functional logistics and communication that support submission planning. This role provides submission leadership by managing the operational aspects of global regulatory submissions to produce high-quality, time-sensitive deliverables in accordance with agreed-upon submission timelines. Additionally, the AD oversees the process for creating and updating the Global Regulatory Operations Submission Content Plan (GSCP) for major regulatory submission final deliverables, ensuring compliance with applicable regulatory agency regulations, guidelines, and specifications (e.g., FDA, EMA, HC, PMDA, Emerging Markets, ICH, CDISC) within defined timelines.
Essential Functions:
Leadership and Strategy
* Provides leadership for the Global Submissions Team ensuring projects are appropriately resourced, partnering with other regional Submission Heads for additional support for resources when needed.
* Provides the Regulatory Submission Management for a lead compound or submission project that has been identified as critical to Eisai's business success.
* Provides management oversight for the Global Submission Management department, supporting the generation, and when necessary, the re-engineering of Eisai "Best Practices" related to global submission management and dossier development in pursuit of optimal processing performance while maintaining full compliance with Health Authority requirements and guideline.
Global Collaboration
* Collaborates with the EU and Japan Heads of Submission Management to optimize resource allocation and implement "follow-the-sun" workflows for timely submissions across all regions.
* Foster strong cross-regional communication and collaboration to support global objectives.
* Promotes a culture of performance and teamwork, with a focus on staff development in technical skills, interpersonal skills, education, and training, enhancing competency and professionalism.
* Maintains visibility within the organization by regularly presenting on various GSM-related topics. This includes showcasing the achievements, ongoing projects, and developments of the GSM organization, as well as emerging trends in eCTD regulatory submissions. Additionally, cultivate positive and constructive relationships with other members of the Global Regulatory Operations (GRO) team and regulatory colleagues.
* Actively participates in agency/industry events regularly, staying abreast of current developments, trends, and technologies, fostering constructive business relations with other industry peers, Health Authority representatives, and critical business partners/vendors.
* Analyzes trends and evaluates the impact of changes in Health Authority requirements for e-submissions, communicating these changes to the relevant areas within Eisai and driving the necessary changes to processes and procedures.
* Ensure the timely completion of all administrative tasks for this position, including but not limited to monthly reports, performance objective setting, performance reviews, and training, for self and staff.
Hands-On Submission Support
* Actively participates in submission planning and execution, including document compilation, publishing, and quality checks.
* Provide technical oversight and troubleshooting for eCTD submissions and related systems.
Operational Excellence
* Ensure consistent application of GSM global procedures and standards.
* Proactively monitors and assess process performance, identifying opportunities for continuous improvement.
Requirements
* Bachelor's degree in scientific or information technology field; advanced degree preferred
* 8+ years of pharmaceutical industry regulatory experience
* 5+ years of experience with submissions management, process development, standards development and compilation of electronic major submissions required
* Proficient with U.S. and EU submission requirements including but not limited to Emerging Markets
* Advance experience with the drug development process and eCTD regulatory submission standards
* Expert understanding of Project Management concepts and techniques
* Ability to apply SOPs regulations pertaining to electronic submissions
* Ability to lead cross-functional team, establish effective relationships with team members and work well in a cross functional team environment
* Advance experience creating timelines for the development and submission of drug filings to regulatory health authorities
* Excellent organizational skills to support multi-task and manage submission timelines in a fast-paced environment with changing priorities
* Well-organized with the ability to multi-task and work with minimal supervision
* Ability to manage change to support organization's effectiveness by implementing change
* Effectively communicates written and verbal communication skills
* Demonstrates strong analytical, problem solving and critical thinking skills with the ability to analyze problems, identify alternative solutions and implement recommendations for resolution.
* Certification is a plus (such as Regulatory Affairs Professional Society (RAPS)
Technical Skills Required
* Advance working knowledge of global regulatory submission standards, publishing software, software validation concepts, and regulatory publishing best practices
* Proficiency in eCTD publishing tools (e.g., Lorenz docu Bridge, Extedo eCTDmanager, or equivalent).
* Strong understanding of ICH guidelines, regional regulatory requirements, and data standards (e.g., CDISC).
* Extensive experience with Regulatory Information Management (RIM) systems and Document Management Systems (e.g., Veeva Vault, SharePoint, Documentum)
* PowerPoint, SharePoint, XML, Adobe Acrobat, ISI Toolbox and eData transfer systems
* Ability to troubleshoot technical issues related to electronic submissions and publishing.
We are open to remote-based, but the preference for this role is a hybrid work arrangement in Nutley, NJ with 3 days a week in office every week (Tuesday, Wednesday. Thursday).
Eisai Salary Transparency Language:
The annual base salary range for the Associate Director, Global Submission Management is from :$159,000-$208,700
Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.
Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.
Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit **********************************************************
Certain other benefits may be available for this position, please discuss any questions with your recruiter.
Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.
Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:
Right To Work
E-Verify Participation
Auto-Apply*REVISED - Associate Director of Composition/Assistant Professor-in-Residence (non tenure-track), Department of English [R0146549]
Associate director job in Maryland
The University of Nevada, Las Vegas (UNLV) appreciates your interest in employment. We ask that you keep in mind the following when completing your application:
Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process.
Required attachments are listed below on the posting. Your application will not be considered without the required attachments.
Please note that applications must be submitted prior to the close of the recruitment.
Once a recruitment has closed, applications will no longer be accepted. If you need assistance or have questions regarding the application process, please contact Human Resources at ************** or *****************
Job Description
The University of Nevada, Las Vegas invites applications for Associate Director of Composition/Assistant Professor-in-Residence (non tenure-track), Department of English [R0146549].
ROLE of the POSITION
The Department of English at the University of Nevada Las Vegas invites applications for an Assistant Professor-in-Residence/ Associate Director of Composition to begin July 1, 2026. This is a 12-month, non-tenure track position at one of the nation's most diverse universities.
The Associate Director of Composition will:
Teach 3-6 credits each regular semester rotated across online first-year composition courses and the pedagogy practicum for new graduate teaching assistants.
Coordinate online composition courses including developing complete model courses, creating instructional resources, acting as liaison with Online Ed and other major stakeholders in online educational initiatives, and coordinating assessment of online classes.
Mentor program instructors and facilitate regular professional development opportunities
Collaborate with faculty and staff to develop, assess, and revise Composition Program curriculum and policies
Engage in ongoing professional development and participate in faculty governance
Although some requirements of the position are virtual, a regular campus presence is required in order to facilitate effective mentoring, collaboration, and program administration. This is a non-tenure-track position, there is a ladder for promotion through the Assistant Professor-in-Residence component of this position.
MINIMUM QUALIFICATIONS
This position requires a PhD in English, Rhetoric and Composition, Technical or Professional Communication, or other related field from an accredited college or university as recognized by the United States Department of Education and/or the Council on Higher Education Accreditation (CHEA).
At least 4 years of experience teaching writing in higher education, including at least 2 years (four semesters) of teaching writing online, is also required. Basic digital media production skills and proficiency in creating accessible materials is required. Credentials must be obtained prior to the start date.
PREFERRED QUALIFICATIONS
Experience administering writing programs and mentoring instructors is preferred. Knowledge of anti-racist, equitable, and inclusive pedagogical and assessment practices is preferred. Understanding of current issues and controversies related to generative AI and experience integrating generative AI policies and practices into curriculum is preferred. Understanding of best assessment practices for online courses is preferred.
COMMITMENT to DIVERSITY
The successful candidate will demonstrate support for diversity, equity and inclusiveness as well as participate in maintaining a respectful, positive work environment.
SALARY RANGE
Salary Competitive with those at similarly situated institutions
BENEFITS OF WORKING AT UNLV
Competitive total rewards package including:
Paid time off, sick leave, and holidays
Excellent health insurance including medical, dental and vision
Comprehensive retirement plans and voluntary benefits programs
No state income tax
Tuition discounts at Nevada System of Higher Education (NSHE) schools
Tuition discounts for spouses, domestic partners, and dependents
PERKS & PROGRAMS
Employee recognition and appreciation programs
UNLV athletics ticket discounts
Statewide employee purchase program discounts
RebelCard discounts on and off campus
Wellness programming for all UNLV faculty and staff at no cost
Opportunity for career advancements to leadership roles
Connect with colleagues with shared interests
Personal and professional development opportunities
A comprehensive onboarding program, Rebels: Onboard
Support and resources available for veteran applicants - contact ********************** or visit our Veterans Webpage.
HOW TO APPLY
Submit a letter of interest, a detailed CV listing qualifications and experience, and the names, addresses, and telephone numbers of at least three professional references who may be contacted. References will not be contacted until the search chair notifies you in advance.
Applicants should fully describe their qualifications and experience, with specific reference to each of the minimum and preferred qualifications because this is the information on which the initial review of materials will be based.
Materials should be addressed to Francisco Ortega and Elaine Bunker, Co-Chairs of the Search Committee.
Although this position will remain open until filled, review of candidates' materials will begin on October 20, 2025 (*REVISED).
Applications must be submitted electronically through Workday. Please note that emailed materials will not be accepted.
Veterans are encouraged to apply. UNLV values the skills of those who have served. Learn more at Veterans Webpage or contact ********************** for support.
For assistance with the application process, please review instructions on How to Apply. For further assistance contact UNLV Human Resources at ************** or *****************.
SPECIAL INSTRUCTIONS FOR INTERNAL NSHE CANDIDATES
UNLV employees or employees within the Nevada System of Higher Education (NSHE) MUST use the “Find Jobs” process within Workday to find and apply for jobs at UNLV and other NSHE Institutions. Once you log into Workday, type "Find Jobs" in the search box which will navigate to the internal job posting site. Locate this specific job posting by typing the job requisition number, "R0146549" in the search box.
If you complete an application outside of the internal application process, your application will be returned and you will have to reapply as an internal applicant which may delay your application.
PROFILE of the UNIVERSITY
Founded in 1957, UNLV is a doctoral-degree-granting institution comprised of approximately 30,000 students and more than 3,600 faculty and staff. To date, UNLV has conferred more than 152,000 degrees, producing more than 130,000 alumni around the world. UNLV is classified by the Carnegie Foundation for the Advancement of Teaching as an R1 research university with very high research activity, and is a recipient of the Carnegie Classification for Community Engagement. The university is committed to recruiting and retaining top students and faculty, educating the region's diversifying population and workforce, driving economic activity through increased research and community partnerships, and creating an academic health center for Southern Nevada that includes the launch of a new UNLV School of Medicine. UNLV is located on a 332-acre main campus and two satellite campuses in Southern Nevada.
Here at UNLV, we have come together and created one of the most affirmative and dynamic academic environments in the country. UNLV sits in the top spot in U.S. News & World Report's annual listing of the nation's most diverse universities for undergraduates. The university has ranked in the top ten since the rankings debuted more than a decade ago. We continue to show our commitment to serving our wonderfully diverse population and building the future for Las Vegas and Nevada.
For more information, visit us on line at: *******************
EEO/AA STATEMENT
The University of Nevada - Las Vegas (UNLV) is committed to providing a place of work and learning free of discrimination on the basis of a person's age (40 or older), disability, whether actual or perceived by others (including service-connected disabilities), gender (including pregnancy related conditions), military status or military obligations, sexual orientation, gender identity or expression, genetic information, national origin, race (including hair texture and protected hairstyles such as natural hairstyles, afros, bantu knots, curls, braids, locks and twists), color, or religion (protected classes). Discrimination on the basis of a protected class, including unlawful harassment, which is a form of discrimination, is illegal under federal and state law. Where unlawful discrimination is found to have occurred, UNLV will act to stop the unlawful discrimination, to prevent its recurrence, to remedy its effects, and to discipline those responsible. Women, minorities, and veterans are encouraged to apply.
TITLE IX STATEMENT
The University of Nevada, Las Vegas, does not discriminate on the basis of sex in any education program or activity that it operates. Non-discrimination on the basis of sex is mandated by Title IX of the Education Amendments of 1972 (20 U.S.C. §§ 1681 et seq.) and the corresponding implementation regulations (34 C.F.R. Part 106). The University's commitment to nondiscrimination in its education programs and activities extends to applicants for admission and employment. Inquiries concerning the application of these provisions may be referred to: Michelle Sposito, J.D., Title IX Coordinator, University of Nevada, Las Vegas, 4505 S. Maryland Parkway, Mail Stop 1062, Las Vegas, NV 89154-1062, Campus Services Building (CSB) Room 246, Telephone: **************; Email: ***************************, or to The Assistant Secretary of the United States Department of Education, U.S. Department of Education, Office for Civil Rights, 400 Maryland Avenue, SW, Washington, D.C. 20202-1100; Telephone: ************** FAX: ************; TDD: **************; Email: **********; or to both.
Information pertaining to the University's grievance procedures and grievance process, including how to report or file a complaint of sex discrimination, how to report or file a formal complaint of sexual harassment, and how the University will respond can be found online at the Office of Equal Employment & Title IX webpage.
SAFETY AND SECURITY STATEMENT
UNLV is committed to assisting all members of the UNLV community in providing for their own safety and security. The Annual Security Report and Annual Fire Safety Report compliance document is available online.
JOB CATEGORY
Administrative Faculty
Yes
Full-Time Equivalent
100.0%
Required Attachment(s)
Submit a letter of interest, a detailed CV listing qualifications and experience, and the names, addresses, and telephone numbers of at least three professional references who may be contacted.
Posting Close Date
05/20/2025
Note to Applicant
This position may require that a criminal background check be conducted on the candidate(s) selected for hire.
HR will attempt to verify academic credentials upon receipt of hiring documents. If the academic credentials cannot be verified, HR will notify the faculty member that an official transcript of their highest degree must be submitted within thirty days of the faculty member's first day of employment.
References will be contacted at the appropriate phase of the recruitment process.
As part of the hiring process, applicants for positions in the Nevada System of Higher Education may be required to demonstrate the ability to perform job-related tasks.
For positions that require driving, evidence of a valid driver's license will be required at the time of employment and as a condition of continued employment.
All document(s) must be received on or before the closing date of the job announcements (if a closing date is provided).
Recruitments that provide a work schedule are subject to change based on organizational needs.
Auto-ApplyCOO
Associate director job in Eldersburg, MD
Job DescriptionDescription:
Do you thrive on turning vision into action and helping teams succeed together? Are you passionate about building strong operations while honoring the people who make the work possible? Do you bring a balance of strategy and hands-on leadership, ready to step into the field as easily as the boardroom? If you are a decisive, collaborative leader who values curiosity and learning as much as results, we want to talk to you!
Our ideal COO is:
•Transparent Communicator - You share direction clearly, encourage dialogue at every level, and listen actively to ensure understanding across the organization.
•Hands-On Leader - You're not confined to an office; you work shoulder to shoulder with the team, respecting every role and valuing the contributions of all employees.
•Curious and Humble - You ask thoughtful questions, observe before acting, and learn from the people around you. You avoid preconceived ideas and adapt by truly understanding how the business operates.
•Accountable and Decisive - You own outcomes, make timely, data-driven decisions without analysis paralysis, and instill confidence by following through from start to finish.
•Strategic Business Partner - You bring strong business acumen, guiding growth, financial health, and long-term planning while championing innovation.
•Empathetic Mentor - You coach and develop talent, celebrate wins, and foster a culture of integrity, humility, and respect.
Our ideal COO combines vision with curiosity, grit with humility. This is a leader who drives results while honoring the heritage of a family-owned business. You'll enhance processes, shape growth, and create harmony between people and performance. At Mid Atlantic Contracting, your leadership will have a direct impact on scaling the company, supporting employees, and building a future where success is shared by all.
RESPONSIBILITIES
The responsibilities of the COO role include, but are not limited to:
Executive Leadership
•Guide the organization toward growth by translating strategic goals into a clear direction.
•Champion a collaborative, team-first environment rooted in respect and accountability.
•Inspire confidence through decisive action and consistent follow-through.
•Foster innovation and process improvement while preserving the company's values.
Management
•Oversee financial performance across the enterprise, including P&L and pro forma planning.
•Strengthen client retention, satisfaction, and acquisition through operational excellence.
•Lead employee growth and retention efforts by mentoring, coaching, and building efficiencies.
•Design and implement effective processes, tools, and metrics for proper labor and staffing levels.
•Manage multiple verticals and divisions, ensuring alignment and clarity across teams.
•Support and manage sales leaders in driving organizational revenue and market expansion.
Accountability
•Hold teams responsible for process adoption and execution.
•Address escalated issues with fairness and clarity, serving as a sounding board and problem-solver.
•Ensure operational initiatives are carried through from concept to completion.
•Balance financial stewardship with people-first decision making.
•Make work engaging and rewarding, reinforcing the company's passion for winning together.
**This is a full-time, in-person position based in the Woodbine, MD area**
Apply through the link: *********************************************************************************
Requirements:
QUALIFICATIONS
Required
•Minimum 5 years in an executive-level role such as COO, VP of Operations, or Director of Operations.
•Experience leading multiple divisions concurrently.
•Experience in a blue-collar service industry, managing diverse teams from hourly field staff to formally trained white-collar professionals.
•Commercial construction background, including fleet, safety programs, purchasing and facilities management.
•Proven financial planning and analysis expertise with P&L management and strategic opportunity development.
•Track record managing sales professionals and organizational growth of $20M-$50M in revenue.
Preferred
•Career progression from field experience into leadership, demonstrating steady growth and success.
•Exposure to light manufacturing.
•Background in privately held or family-owned businesses.
•Enterprise risk management knowledge, including insurance, bonding, and HR risk oversight.
•Experience guiding growth from $20M-$100M in revenue.
•Involvement in merger and acquisition integration.
•Government contracting experience.
Desired
•Exposure to multiple trades, including general contracting, wireless infrastructure, concrete contracting, metal fabrication and contract manufacturing.
•Experience scaling organizations from 10 employees to 500 employees.
Associate Director for Career Pathways & Employer Engagement - McDaniel College
Associate director job in Westminster, MD
The Associate Director for Career Pathways and Employer Engagement leads the external-facing career development efforts, building and maintaining relationships with employers and alumni to expand opportunities for students. This role coordinates professional pathway showcases, career fairs, and networking events, and promotes internship, job and experiential learning opportunities. This position will join a team-oriented office comprised of a staff team dedicated to delivering on the McDaniel Commitment, signature program for student development at McDaniel College. This position supports the overall mission of career development and experiential learning within the Center for Experience and Opportunity (CEO) and reports to the Executive Director.
Key Responsibilities
* Cultivate and manage relationships with employers to increase recruitment and internship opportunities.
* Engage the regional employer and community member landscape to effectively engage students and strategically involve partners in on and off-campus experiences.
* Develop and implement a comprehensive employer relations and industry partnerships strategy to increase the number and quality of job, internship, externship, and placement opportunities for students and alumni.
* Build and maintain relationships with key employers and industry leaders to promote the College as the premier local/regional higher education talent repository.
* Conduct employer site visits to assess quality of placements and internships for McDaniel students.
* Oversee the coordination of college-wide career and experiential learning events/activities involving employers and external partners
* Plan and execute career fairs, networking events, and employer panels.
* Engage alumni in career development efforts through mentorship, events, and outreach.
* Teach one "My Career" class each semester.
* Serve as co-chair of the "My Career" Committee.
* Collaborate with Career Education on advising, career fairs, Professional Pathway Showcases, and other events.
* Conduct assessment and reporting for employer engagement initiatives.
* Research and stay informed on industry knowledge and trends, with a focus on positioning students to model current best-in-class Career Readiness Competencies.
* Participate in professional development activities and regional alliances to enhance programs and contribute to a best practices experiential learning environment.
* Report work weekly, semesterly, annually and in ways that support dashboard delivery.
* Represent the office at various campus events, committees and task forces based on assignment and interest.
* Manage Handshake platform and promote employment and experiential learning opportunities.
* Other duties as assigned.
Information Security Role: Data User
* Follow the policies and procedures established by the appropriate Data Stewards.
* Comply with federal and state laws and regulations as well as College policies, procedures, and standards associated with the College computing resources and institutional data used.
* Use institutional data only as required for the conduct of College business within the scope of employment.
* Implement safeguards prescribed by appropriate Data Stewards for Limited Access and Restricted Data.
* Ensure the appropriateness, accuracy, and timeliness of institutional data used for the conduct of college business.
* Report any unauthorized access, data misuse, or data quality issues to the appropriate Data Steward for remediation.
* Accept and complete the confidentiality statement yearly if access includes Restricted data.
* Report any suspected data breach to the CIO and the IT Help Desk as soon as possible.
Campus Security Authority Responsibilities
* Designated as a "mandatory reporter," otherwise known as a Campus Security Authority, to report any information about potential, active or previously occurring crime(s) on campus as defined through federal regulation to the Department of Campus Safety immediately upon learning about them.
Requirements:
Qualifications
* Master's degree required.
* 3 to 5 years of experience in employer relations, event planning, and partnership development.
* Excellent communication and relationship-building skills.
* Excellent organizational, multi-tasking, and problem-solving skills.
* Ability to work effectively in a collaborative, fast-paced work environment, to perform effectively with fluctuating workload, and to meet established deadlines.
* Demonstrated ability to work independently as well as cooperatively with others and provide excellent customer service to students and to all members of the campus community.
* Self-motivated, flexible, and possessing a strong work ethic.
* High level of comfort with presenting to small and large groups and with the technology-rich work environments requiring the use of Handshake, the Microsoft Office suite and various social media platforms.
* Availability to run occasional evening and weekend programming.
Working Conditions
* While performing the duties of this job, the employee is routinely working in a normal office environment with minimal exposure to adverse conditions.
Physical Abilities
The physical demands described below are representative of those that must be met by an employee to successfully perform the essential functions of this job:
* Limited lifting involved but not more than 10 pounds at a time.
* Finger dexterity for typing and use of other office equipment.
* Standing and/or sitting, walking, keyboarding, talking and hearing are required.
* Close visual acuity.
* Subject to inside and outside environmental conditions.
Additional Information:
McDaniel College, in compliance with federal and state laws and regulations, does not discriminate in the recruitment, admission, and employment of students, faculty, and staff in the operation of any of its educational programs and activities. McDaniel College will not tolerate any discrimination or harassment on basis of any protected status including protective hairstyle, race, religion, color, ancestry or national origin, disability, age, sex, gender, gender identity, gender expression, sexual orientation, pregnancy, military status, genetic information, marital status, veteran's status, or any other actual or perceived legally protected characteristics.
Application Instructions:
Completed applications must include the following: cover letter addressing position qualifications and related experience, resume, portfolio, names and contact Information of three professional references, a completed job application. Review of applications begins immediately. The position will remain open until filled.
Please click the Apply Now button below to begin your application.
Associate Director, Global Product Quality - Biologics
Associate director job in Rockville, MD
The Associate Director, Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at CMOs under contract by Otsuka to ensure that they are manufactured, packed, labelled, stored, and transported in a controlled way that is in accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role will direct Biologics Quality Assurance support, including oversight of upstream and downstream biologics manufacturing processes, ensuring compliance with biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for Otsuka's patients. This role will also work collaboratively with other functional departments across Otsuka Affiliates and Subsidiaries to maintain the effectiveness of the Otsuka Quality Systems that support OPDC-sponsored clinical studies as well as drive continuous improvement.
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+ Responsible for directing quality oversight of GMP contract manufacturers of Otsuka clinical and commercial products.
+ Develops comprehensive quality strategies for complex biologic development programs that address unique manufacturing challenges.
+ Establishes and maintain the effectiveness of Quality Systems for managing the batch record review and release process Quality Management Activities supporting all phases of clinical development as well as Commercial Product (API, drug product, and final finished product).
+ Transforms biologic manufacturing quality challenges through innovative approaches that maintain product integrity while optimizing operational efficiency.
+ Works collaboratively within the Global Quality Dept. and other functions within OAPI and OPDC to assure Compliance to ensure continuous improvement and compliance.
+ Manages reports and trends to the Management Representative to help in the preparation of Management reviews and/or other ad hoc reporting requests.
+ Establishes and maintains Standard Operating Procedures, work instructions, forms, templates and other documents associated with the systems noted above.
+ Improves supplier quality performance for batch record review and release process for OAPI GMP release of Contract Manufacturers operations supporting clinical and commercial products.
+ Interfaces with Contract Manufacturers/Laboratories, Tech Ops, Technical Services and Supply Chain Sourcing to drive Quality improvements that minimize the Costs of Quality, specifically component, materials or finished product deviations, OOS incidents, rejects, etc.
+ Represents global quality during execution of product technical transfer activities to ensure all aspects of the transfer are conducted per cGMP.
+ Assists in conducing audits of Contract Manufacturers/Laboratories (as part of an audit team) to ensure compliance with OAPI and OPDC requirements as well as applicable regulatory requirements.
+ Responsible for reviewing, drafting, and augmenting existing Quality agreements with external service providers to assure that full compliance and best practices as identified by Otsuka are communicated and continuously met.
+ Serves as a Global Quality Product Champion with a focus on ensuring the quality of our biologics products, monitoring, and escalation of any situations with potential negative impacts on clinical study supplies, supply chain for commercial products, or patient safety.
**Qualifications**
Required
+ Bachelor's degree in Chemistry, Biology or other Physical Sciences.
+ Ten years of combined and/or pharmaceutical manufacturing, QA or QC assurance roles managing and directing quality oversight of commercial product and development project activities.
+ Seven years of product quality experience performing batch review and release activities of suppliers or contract manufacturers or equivalent preferred supporting commercial products and/or development projects.
+ Proven experience with biologics GMP manufacturing, including upstream (cell culture, bioreactors) and downstream (purification, filtration, formulation) processes.
+ Expertise in conducting root cause investigations and driving CAPA implementation.
+ Ability to supervise multiple direct reports and projects in a fast-paced environment.
+ Demonstrated success in working on and leading cross functional teams.
+ Experience with Pre Approval Inspections for NDAs and BLAs.
+ Experience in driving continuous improvement projects.
+ TrackWise Experience.
+ Excellent interpersonal and communication skills.
+ Position requires approximately 20% domestic travel; Occasional international travel may also be expected.
Preferred
+ Advanced degree in Biology or other Physical Sciences.
+ Experience with quality oversight of controlled substances.
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $146,955.00 - Maximum $219,650.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.