Senior Technician Specialist jobs at AbbVie - 298 jobs
Senior MSL, Nephrology - IgA Nephropathy Specialist
Upsher-Smith 4.7
San Rafael, CA jobs
A leading biotechnology company is seeking a Senior Medical Science Liaison focused on Nephrology programs. This role entails establishing relationships with healthcare professionals, executing the medical affairs strategy, and delivering scientific information. Candidates should have a minimum of 3-4 years in a similar position, an advanced life sciences degree, and strong communication skills. The position offers a competitive salary and robust benefits, reflecting the company's commitment to employee growth and well-being.
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$54k-104k yearly est. 1d ago
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Cloud Technical Lead
Abbott Laboratories 4.7
San Diego, CA jobs
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
Career development with an international company where you can grow the career you dream of.
Employees can qualify forfree medical coverage in our Health Investment Plan (HIP) PPOmedical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
The Cloud Technical Lead position is within our Infectious Disease business unit located at the Towne Centre site in San Diego, California. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.
This role will be responsible for technical implementation of cloud solutions.
Working closely with local and remote software engineering teams (international) developing software products and platforms as well as supporting current products. This role will promote Agile product development principles and foster continuous improvement. This individual must be a positive, “can-do” leader with exceptional technical background, who possesses the skills of pulling together ideas and suggestions, shaping them into a vision, and then implementing them in a product. This very hands-on position would require a focus on details and collaboration with the cloud software development team.
The Cloud Technical Lead should demonstrate good communication and people skills, so they can collaborate well within the team and across multiple departments and business units. They should also demonstrate willingness and potential to motivate and grow other team members.
What You'll Work On
Provide technical leadership to a global team of software developers to create high quality cloud solution.
Collaborate with other teams in the organization (local and remote) to coordinate on delivery timelines.
Facilitate decisions on scope of work, duration of tasks, and product requirements.
Evaluate current development processes and provide recommendations for improvements.
Understands and is aware of the quality consequences which may occur from the improper performance of the products.
Identify key barriers/core problems and apply problem-solving skills in order to deal creatively with complex situations.
Troubleshoot and resolve complex problems, and make decisions under conditions of uncertainty, sometimes with incomplete information, that produce effective end results.
Collaborate on establishing best practices in software and systems that lead to efficient development, support high-quality software, and are compliant with our Quality Management System
Use strong technical abilities and able to suggest multiple solutions to problems.
Responsible for the development of complex technical project plans and schedules covering all engineering activities.
Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; build productive internal/external working relationships
Carries out duties in compliance with established business policies
Other duties as assigned, according to the changing needs of the business
Required Qualifications
Hands on experience developing Cloud solutions. Experience in using Agile methodologies (e.g. SCRUM, Kanban, TDD, etc.)
10 years of experience in systems and/or software development involving interoperability of connected devices. (Python, React and T-SQL)
Bachelor of Science, Computer Engineering, Computer Science or equivalent experience (MS preferred) plus 5 years' experience.
Preferred Qualifications
Hands-on experience with Azure AD\Entra ID or similar identity platforms such as Okta\Identity Serve and etc.
Good understanding of Authentication\Authorization and OAuth 2.0\Open ID Connect standards.
Hands-on experience with Azure Cloud Services such as Kubernetes service, App Service, Azure Function, App Gateway, Azure Blob Storage, Log Analytics, Azure Key Vault, Azure Data Factory, API Gateway, Event Hub.
Experience with Infrastructure as a Coding technologies such as Terraform.
Experience with CI\CD technologies such as Azure DevOps\Jenkins.
Experience with Static Code Analysis such as Veracode or Fortify on Demand.
Good understanding front end frameworks such as React or Angular.
Proficiency with at least one of modern application development languages, such as Python or C#.
Experience with REST API's technologies such as FastAPI\ASP.NET Core Web API.
Experience with network protocols, integration and integration testing, and cybersecurity
Proficient with Medical Device regulations (ISO 13485, ISO 14971, IEC 62304, 21 CFR part 820.30-Design Controls, FDA SW Guidelines…).
Experience in delivering products for the Medical Device IVD industry.
Experience with testing techniques for cloud solutions.
Strong written, verbal, interpersonal and presentation skills.
Good understanding of the TLS\HTTPS REST\SOAP protocols.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: **********************
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at *************** on Facebook at ************************ and on Twitter @AbbottNews.
The base pay for this position is $112,000.00 - $224,000.00. In specific locations, the pay range may vary from the range posted.
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$112k-224k yearly 5d ago
Onboarding Specialist
Octapharma Plasma, Inc. 3.8
Charlotte, NC jobs
Octapharma Plasma offers professional opportunities that make a meaningful difference. We enhance the lives of patients who need our life-saving medicines. We reward the donors who provide the plasma we collect to make them. And we inspire growth and development in the teams at our donation centers, offices, and labs. We invite you to do the same in this role:
Onboarding Specialist
This Is What You'll Do:
Plan and coordinate the logistics of new employee onboarding, including scheduling and preparing materials.
Conduct orientation sessions to introduce new hires to the company's culture, values, policies and procedures.
Schedule and coordinate onboarding activities, providing guidance and support to new hires throughout the process.
Ensuring completion of paperwork and following all legal and administrative compliance when onboarding candidates.
Assist new hires with completing the necessary paperwork, including employee forms, benefits enrolment, and IT setup.
Processes I-9 and E-Verify requests.
Processes background checks and drug screens.
This Is Who You Are:
Excellent interpersonal skills, strong written and verbal communication skills.
Highly ambitious and ability to think outside of the box.
Eager to share new ideas and contribute to a team.
Self-motivated and willing to assume the initiative.
Attentive to every detail.
Capable of thriving while working independently.
This Is What It Takes:
2+ years of experience in onboarding and recruitment with a proven track record of successful onboarding processes and employee retention.
Strong knowledge of onboarding best practices, HR policies and procedures, and employment laws and regulations to ensure compliance during the onboarding process.
Strong organizational skills to manage and streamline the onboarding process efficiently.
Excellent communication and interpersonal skills to build rapport with new employees and establish a positive onboarding experience.
Attention to detail and organizational skills to coordinate and manage multiple onboarding processes simultaneously.
Adaptability and flexibility to accommodate the diverse needs and backgrounds of new employees.
Ability to collaborate and work effectively with remote team members with prior experience in corporate onboarding.
Proficiency in Microsoft Office Suite.
Proficiency in using HRIS systems and experience with different applicant tracking systems.
May require travel to assist field locations with recruitment.
We're widely known and respected for our benefits and for leadership that is supportive and hands-on.
Formal training
Outstanding plans for medical, dental, and vision insurance
Health savings account (HSA)
Employee assistance program (EAP)
Wellness program
401 (k) retirement plan
Paid time off
Company-paid holidays
Personal time
More About Octapharma Plasma, Inc.
With donation centers and team members throughout the U.S., Octapharma Plasma, Inc. collects plasma to create life-saving medicines for patients worldwide. We are growing at an impressive pace, and so is the positive impact of our work. Our community relies on teamwork, compassion, and expertise to get things done the right way, while making a meaningful difference in the lives we touch.
INNER SATISFACTION.
OUTSTANDING IMPACT.
$33k-58k yearly est. 4d ago
REMOTE Caregiver Training Specialist (BCBA)
Res-Care, Inc. 4.0
Charlotte, NC jobs
Our Company SpringHealth Behavioral Health and Integrated Care is to provide support for the caregiver training/education. NO- Caseload Oversight NO- RBT Superivision NO- Treatment plan writing NO- Scheduling headaches NO- Administrative Mazes.
Qualifications:
Must be a Board Certified Behavior Analyst (BCBA). Must have Strong communication and virtual presentation skills.
Responsibilities
* Conduct comprehensive assessments of children with Autism Spectrum Disorder (ASD) to evaluate behavior, skills, and needs.
* Develop individualized Behavior Intervention Plans (BIPs) based on assessment results and collaborate with multidisciplinary teams to refine diagnostic and therapeutic approaches.
* Design and implement evidence-based Applied Behavior Analysis (ABA) interventions tailored to each client's unique needs and goals.
* Continuously monitor and adjust treatment plans to reflect progress and address emerging needs.
* Apply ABA techniques to improve social, communication, academic, and daily living skills.
* Implement strategies to reduce maladaptive behaviors and promote positive behavior changes.
* Collect and analyze data on behavior and progress to evaluate the effectiveness of interventions and make data-driven decisions.
* Maintain detailed records and prepare reports to track patient progress and communicate with stakeholders.
* Educate and support parents and caregivers in understanding ASD and implementing behavioral strategies at home.
* Provide guidance on managing challenging behaviors and enhancing communication and social skills.
* Work closely with other professionals, including speech therapists, occupational therapists, and educators, to ensure a cohesive approach to treatment.
* Participate in interdisciplinary team meetings and share insights to optimize care plans and outcomes.
* Supervise and mentor Registered Behavior Technicians (RBTs) and other direct support staff, providing training and feedback to ensure high-quality service delivery.
* Conduct regular performance reviews and offer professional development opportunities for team members.
* Engage with community resources and support networks to enhance the client's social and environmental integration.
* Ensure that all interventions and practices adhere to ethical guidelines, professional standards, and regulatory requirements.
* Stay current with developments in the field of behavior analysis and autism treatment, integrating new research and best practices into clinical work.
* Address and manage crisis situations effectively, utilizing de-escalation techniques and ensuring the safety of the client and others.
* Complete and finalize daily clinical documentation within SpringHealth's EHR.
* Assist in developing procedures for training materials for staff with the purpose of enhancing programs for clients and ensuring that program operations are in compliance with established guidelines.
* Continued education on behaviorally based interventions & techniques to stay competitive in the field.
* Complete monthly & quarterly notes outlining the client's progression through goals.
Qualifications
* Must be a Board Certified Behavior Analyst (BCBA) in good standing with the BACB.
* Review and interpret highly technical information; write technical materials; and/or speak persuasively to implement desired actions; and analyze situations to define core issues and draw conclusions.
* Specific knowledge-based competencies required to satisfactorily perform the functions of the job include age-appropriate activities/behaviors; understanding of CPT codes/payor rules/regulations/policies; language grammar/punctuation/spelling/vocabulary; and research-based accepted treatment modalities and assessment.
* Must have reliable transportation.
* Ability to perform physical tasks, including standing for extended periods, infrequent lifting to 50 pounds, frequent pushing, pulling, reaching, turning, twisting, bending, stooping, and squatting, walking, and climbing.
About our Line of Business
SpringHealth Behavioral Health and Integrated Care, an affiliate of BrightSpring Health Services, offers a holistic approach and integrated care for people with cognitive, developmental, or intellectual disabilities who often need additional resources. The behavior analysts, therapists, social workers, counselors, and psychologists at SpringHealth combine their expertise to deliver high-quality behavioral services for clients to live more positive, active, and social lives. For more information, please visit ******************************* Follow us on Facebook and LinkedIn.
Salary Range
USD $35.00 - $45.00 / Hour
$35-45 hourly Auto-Apply 58d ago
IPQA Level II
Aurobindo Pharma Ltd. 4.4
East Windsor, NJ jobs
Aurobindo Pharma USA, Inc. is a generic pharmaceutical manufacturer and distributor and is a wholly owned subsidiary of Aurobindo Pharma Limited, a leading generic pharmaceutical company based in India. Headquartered in HITEC City, Hyderabad, India, founded in 1986 and becoming a public company in India in 1992.
AuroPackaging (APK) is a division of Aurobindo USA that plays a primary role in converting the Bulk from our manufacturing sites to Finished Goods (FG) as per requirements. AuroPackaging was founded in 2018 as part of a group of companies that has a long history of excelling in generic pharmaceutical product development and manufacturing. The support and expertise of our parent organization has given AuroPackaging a jump start in building a solid pharmaceutical portfolio very quickly. AuroPackaging's aim is to provide healthcare at economical prices to make a healthier world to live in.
Job Overview
IPQA Associate Level II will support and assist activities related to the production of pharmaceutical products in accordance to current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs) and batch record specification. The IPQA Associate shall assure compliance with all standards and regulatory guidelines.
Responsibilities
* Collaborates with other production staff and Departments.
* Accurately and consistently completes and documents batch records/other required paperwork.
* May provide on the job training and day to day guidance to other nonexempt personnel.
Qualifications - Skills & Requirements
* Good communication skills and capable of communicating with all levels
* Be available for overtime, including weekends, as needed for production support.
* A familiarity with cGMPS, CFRs, OSHA and FDA regulations.
Education & Experience
* High School Diploma or equivalent GED.
* Up to 4 years of experience performing in-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment.
Compensation
Min
USD $24.00/Hr.
Max
USD $28.00/Hr.
Physical Requirements
WAREHOUSE OR PRODUCTION POSITION - While performing the duties of this job the employee is required to: Regularly lift and/or move objects 10-50lbs Frequently required to stand, walk, stoop, kneel, crouch or crawl Occasionally required to sit and climb or balance Specific vision abilities required for this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust and focus The worker is subject to environmental conditions. Protection from weather conditions but not necessarily from temperature changes The worker is subject to both environmental conditions. Activities occur inside and outside Medium work Exerting up to 50 pounds of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects.
Additional Physical Requirements
No Additional Requirements
Blood/Fluid Exposure Risk
Category III: Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.
$24-28 hourly Auto-Apply 50d ago
Senior Flavorist, Citrus, North America
DSM 4.3
Princeton, NJ jobs
At dsm-firmenich, we're looking for a Senior Flavorist to help craft world-class flavors that don't just taste exceptional-they tell stories, spark emotions, and create unforgettable experiences. You will help our customers bring their brands to life by blending science, creativity, and a deep understanding of consumer insight. Whether it's a nostalgic favorite or a bold new creation, our flavor innovations set the standard for excellence in taste, and we want you to be a part of it.
Your Key Responsibilities:
* Create and optimize flavor formulations across a variety of categories, with a focus on taste performance, stability, and regulatory compliance
* Serve as one of the subject matter expert in citrus flavor development for North America, working closely with the NA citrus team and the global citrus creation team
* Present flavor concepts and technical insights to key clients in North America, supporting business development and customer satisfaction
* Collaborate with cross-functional teams including sensory, applications, and regulatory to ensure successful project execution
* Mentor junior flavorists and contribute to knowledge sharing and best practices within the global flavorist community
* Stay informed on market trends, raw material innovations, and sustainability initiatives.
We Bring:
* A rich history and a promising future of bold scientific innovation and passionate creation with our customers
* Opportunity to grow by encouraging and supporting curiosity and an open mindset within a collaborative team environment
* A culture that prioritizes safety and well-being, both physically and mentally
* The opportunity to work for a company where sustainability is much more than a claim and is core to our strategy and purpose
* An eagerness to be one team and learn from each other to bring progress to life and create a better future
* We offer competitive pay, career growth opportunities, and outstanding benefit programs
You Bring:
* Minimum 10 years of experience in flavor creation, with demonstrated expertise in citrus and other key flavor profiles for sweet and beverage applications
* Strong understanding of flavor stability, particularly in citrus applications
* Excellent sensory evaluation skills
* Proven ability to communicate effectively with clients and internal stakeholders
* Bachelor's or Master's degree in Food Science, Chemistry, or a related field
* Willingness to travel within North America for client meetings and innovation workshops
The salary or hourly wage scale provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education, or training, and primary work location. Salary $176,300.00-$190,000.00.
In addition to base salary, we also offer a comprehensive total rewards package, inclusive of annual incentive pay, a retirement savings plan, health care coverage, paid time off, recognition programs and a broad range of other benefits. All benefits and incentives are subject to eligibility requirements.
About dsm-firmenich
At dsm-firmenich, we don't just meet expectations - we go beyond them.
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future.
Because real progress only happens when we go beyond, together.
The application process
Interested in this position? Please apply online by uploading your resume in English. We anticipate the application window for this opening will close on October 6, 2025
Inclusion, belonging and equal opportunity statement
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work.
Agency statement
We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.
$176.3k-190k yearly 32d ago
Senior Technical Specialist- Security Architect (2 Year Project)
Training Specialist/ Senior Training Specialist (Instructional Design)
Brookhaven Science Associates 3.7
New York jobs
Brookhaven National Laboratory is committed to employee success and we believe that a comprehensive employee benefits program is an important and meaningful part of the compensation employees receive. Review more information at BNL | Benefits Program
Organizational Overview:
Brookhaven National Laboratory seeks a Nuclear Training Specialist to support the nuclear training and qualifications program. This position resides within the Human Resources Department and is matrixed to the Nuclear Safety Division. The position is based in Upton, New York, 60 miles east of New York City in Suffolk County. BNL has approximately 2,800 employees and is growing. BNL is a government-owned, contractor-operated facility funded through the United States Department of Energy (DOE). Visit *********** for more information.
BNL's Nuclear Safety program is being expanded to address the nation's growing demand for critical medical radioisotopes. DOE has designated this as a Mission Essential Function for BNL, and increased production capacity will require operation under a nuclear regulatory structure. In support of this effort, the Nuclear Safety program elements ensure compliance with 10 CFR 830, Nuclear Safety Management, and all associated DOE Directives.
The Nuclear Safety Division is a part of the Environment, Safety, and Health Directorate. Ensuring regulatory compliance and safe operations is the ESH mission. ESH staff support the overall BNL mission by providing expertise that ensures safe and efficient work processes during scientific research, reduces the likelihood of human error, and manages regulatory programs that preserve the safety and health of BNL employees, the public, and the environment.
Position Description:
The Training and Organizational Development team is an integral part of the Human Resources Directorate. It serves as a center of excellence for Leadership Development, Training and Qualifications, and Nuclear Safety Training. In this role, you will support the development, evaluation and maintenance of the nuclear training and qualification program. The role reports to the Nuclear Training Manager. As part of our team, you will work in a research environment with other training and nuclear safety professionals, collaborating with cross-disciplinary teams to support training for BNL's Radionuclide Research and Production Laboratory (RRPL) and future nuclear facilities.
Essential Duties and Responsibilities:
Responsibilities include, but are not limited to:
* Serve as a training specialist and instructional technologist, responsible for the design, maintenance, and development of e-learning and in-person courses to support nuclear safety training
* Create course content, training packages, and develop interactive learning modules; structure curriculum based on learning objectives
* Develop and maintain nuclear facility qualification cards and ensure training records are entered into the electronic records database
* Periodically evaluate the efficacy of training output during the design, development, implementation, and observations of performance, and provide improvement recommendations to the Nuclear Training Manager and line management
* Maintain assigned training and qualification requirements per the Nuclear Training and Qualification Program Description
* Support the Continuing Training Program for assigned nuclear facilities positions to assure qualifications are maintained
* Ability to oversee and manage continuing training programs
* Coordinate involvement of line organization personnel for the SAT development of training materials; conduct and update the SAT process for specific positions and training courses applicable
* Perform needs assessments to evaluate training and identify gaps
* Coordinate, conduct, and document table-top analysis
* Process training exceptions, extensions, and waivers, as requested by line management; providing updates to management on continuation of personnel training
* Review job analyses and job task lists on a recurring basis to determine if revision is necessary; support management and personnel by identifying and executing training requirements
* Responsible for the examination review and approval process which includes developing written and online exams and documenting linkage of test items to tasks and objectives, preparing exam keys, and acting as exam administrator/proctor
Required Knowledge, Skills, and Abilities:
* Bachelor's Degree in education/training or equivalent experience, generally on the basis of 2:1 (experience: college) years
* Bachelor's coursework and/or training must include education or training with a focus on Systematic Approach to Training (SAT) process including analysis, design, development, implementation, and evaluation and/or (ADDIE) model (Analysis, Design, Development, Implementation, Evaluation)
* A minimum of 4 years relevant work experience in delivering and designing training programs
* Hands-on experience with classroom and web-based training design and delivery
* Hands on experience with instructional design and online course development tools such as Articulate Storyline, Rise, and similar
* Ability to manage multiple projects independently and deliver quality training materials that meet regulatory and industry requirements
Preferred Knowledge, Skills, and Abilities:
* Ten (10) years of relevant professional experience
* Experience in instructional design within related fields (scientific or laboratory environment) is a plus
* Industry certifications in instructional design, curriculum development, performance improvement, project management, and content-specific certifications as appropriate
* Familiarity and experience with DOE 426.2A nuclear training requirements
* Strong interpersonal and communications skills
* Demonstrated ability to think strategically and work collaboratively
ENVIRONMENTAL, HEALTH & SAFETY REQUIREMENTS:
* Ability to work at a computer for extended periods of time
Other information
* Please include in your cover letter a description of any coursework or training you have completed in the Systematic Approach to Training (SAT) methodology and/or (ADDIE) model (Analysis, Design, Development, Implementation, Evaluation)
* Work arrangement is onsite, with telework options available
* This position is not eligible for visa sponsorship
Brookhaven National Laboratory is committed to providing fair, equitable and competitive compensation. This is a multi-level role and the full salary range for this position is $80300 - $130000 / year. You will be placed at the level and salary commensurate with your experience. Salary offers will be commensurate with the final candidate's qualification, education and experience and considered with the internal peer group.
Brookhaven National Laboratory requires all non-badged personnel including visitors to produce a REAL-ID or REAL-ID compliant documentation to access Brookhaven National Laboratory - view more information at ***********/real-id. This is due to nationwide identification requirements for federal site access as required by the federal REAL ID Act. Those not in possession of a REAL ID-compliant document will not be permitted to access the site which includes access to the Laboratory for interviews.
About Us
Brookhaven National Laboratory (***********) delivers discovery science and transformative technology to power and secure the nation's future. Brookhaven Lab is a multidisciplinary laboratory with seven Nobel Prize-winning discoveries, 37 R&D 100 Awards, and more than 70 years of pioneering research. The Lab is primarily supported by the U.S. Department of Energy's (DOE) Office of Science. Brookhaven Science Associates (BSA) operates and manages the Laboratory for DOE. BSA is a partnership between Battelle and The Research Foundation for the State University of New York on behalf of Stony Brook University. BSA salutes our veterans and active military members with careers that leverage the skills and unique experience they gained while serving our country, learn more at BNL | Opportunities for Veterans at Brookhaven National Laboratory.
Equal Opportunity/Affirmative Action Employer
Brookhaven Science Associates is an equal opportunity employer that values inclusion and diversity at our Lab. We are committed to ensuring that all qualified applicants receive consideration for employment and will not be discriminated against on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, status as a veteran, disability or any other federal, state or local protected class. BSA takes affirmative action in support of its policy and to advance in employment individuals who are minorities, women, protected veterans, and individuals with disabilities. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. *VEVRAA Federal Contractor
BSA employees are subject to restrictions related to participation in Foreign Government Talent Recruitment Programs, as defined and detailed in United States Department of Energy Order 486.1A. You will be asked to disclose any such participation at the time of hire for review by Brookhaven. The full text of the Order may be found at: ********************************************************************************************
$80.3k-130k yearly Auto-Apply 60d+ ago
Customer Success & Training Specialist - Scientific Products | Union, MO
DSM 4.3
Union, MO jobs
Customer Success & Training Specialist - Scientific Products Union, MO Join a dynamic team supporting customers with technical expertise, product training, and hands-on problem solving. This role blends science, strategy, and customer engagement across a global industry leader. It's a chance to grow your skills, lead impactful projects, and shape the future of food safety solutions.
This position supports our Romer Labs division, a global leader in innovative diagnostic solutions for food and feed safety. With a focus on mycotoxins, food allergens, GMOs, and microbial contaminants. Making the World's Food Safer romerlabs.com
Your key responsibilities
* Provide sales and technical customer support, including troubleshooting, complaint management, and customer-specific validations.
* Deliver product training to customers and internal sales teams via onsite visits, webinars, and continuous learning programs.
* Design and execute experiments, analyze data, and generate technical reports and recommendations based on scientific methodologies.
* Support regional marketing by sharing competitive insights, conducting webinars, and presenting at industry events and conferences.
* Lead technical involvement in complaint and recall processes while contributing to training content and troubleshooting resources.
* Stay current on industry trends and regulatory standards.
We offer
* Unique career paths across health, nutrition and beauty - explore what drives you and get the support to make it happen
* A chance to impact millions of consumers every day - sustainability embedded in all we do
* A science led company, cutting edge research and creativity everywhere - from biotech breakthroughs to sustainability game-changers, you'll work on what's next
* Growth that keeps up with you - you join an industry leader that will develop your expertise and leadership
* A culture that lifts you up - with collaborative teams, shared wins, and people who cheer each other on.
* A community where your voice matters - it is essential to serve our customers well.
You bring
* Bachelor's degree in a scientific related field; or Associates degree plus 2-3 years of expereince
* A strong background in technical sales support, complaint management, and customer troubleshooting
* Experience delivering product training to both customers and internal teams (in-person and virtual)
* Ability to design experiments, analyze data, and translate results into clear, actionable insights
* Skilled in creating technical content and presenting at industry events, webinars, and conferences
* Familiarity with regulatory standards and a passion for staying current with industry trends
* Willingness to travel up to 30%, with flexibility for seasonal demands
The salary or hourly wage scale provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education, or training, and primary work location. Salary $48,700-70,000.
In addition to base salary, we also offer a comprehensive total rewards package, inclusive of annual incentive pay, a retirement savings plan, health care coverage, paid time off, recognition programs and a broad range of other benefits. All benefits and incentives are subject to eligibility requirements.
About dsm-firmenich
At dsm-firmenich, we don't just meet expectations - we go beyond them.
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future.
Because real progress only happens when we go beyond, together.
Inclusion, belonging and equal opportunity statement
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work.
Agency statement
We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.
$48.7k-70k yearly 32d ago
Senior Veterinary Specialist (Dermatology)
Zoetis 4.9
Remote
Role Description
Veterinary Specialist - Board-Certified Dermatologist
About Us: Zoetis has a team of talented specialists supporting key therapeutic areas that includes 4 board-certified dermatologists. We are dedicated to providing our customers and the veterinary profession with expert contemporary medical education and scientific support, helping them to deliver the best care possible for pets.
View the Zoetis Specialist team introduction video.
Role Overview: As a Field Dermatologist, you'll be a key player in educating veterinarians, focusing on disease state, diagnosis, and management of allergic and atopic dermatitis. The position is highly collaborative, working closely with field colleagues, while also being an advisor to business leadership and headquarters teams on products, services, and future pipeline products in Dermatology.
Key Responsibilities:
Education & Support:
Partner with field colleagues to deliver engaging educational and clinical presentations on dermatology.
Provide balanced, science-based product information to veterinarians centered on best medicine.
Adapt your content and communication to meet the unique needs of each customer.
Create innovative content, sharing your insights and experience to support and grow the Zoetis Dermatology Portfolio.
Professional Engagement:
Build a reputation as a trusted advisor to Zoetis colleagues, veterinary healthcare teams, KOLs and corporate partners.
Be recognized as a sought-after and credible speaker able to connect with audiences in varied settings, from a roundtable discussion to delivering a keynote address at major conferences.
Establish strong relationships with dermatologists in private practice, at veterinary colleges and within professional organizations.
Be active in professional/specialty/customer organizations by serving on committees, boards and commissions or as an officer or speaker on the organization's behalf.
Business, Marketing & Training Support:
Provide expert opinion on emerging treatment guidelines and protocols for integration into brand/business strategy and tactics.
Be the subject matter expert advising marketing teams on technical and clinical aspects of dermatology.
Have an active role in developing and delivering training programs for sales and technical colleagues.
Be prepared to mentor colleagues across business units, sharing your experience and insights.
Zoetis Values and Personal Development
Demonstrate Zoetis core beliefs and behaviors.
Fully embrace Zoetis efforts and initiatives in Diversity, Equity &Inclusion, and Sustainability
Lead with influence by example, with actions aligned to Zoetis mission and values.
Constantly seek ways to improve Zoetis and take leadership in identifying continuous improvement initiatives by proactively integrating insights into future engagements.
Maintain comprehensive knowledge and understanding of all scientific and medical information relative to the dermatology and actively maintain a personal development plan that supports career aspirations.
Qualifications:
Doctor of Veterinary Medicine (DVM) or equivalent.
Board certification in dermatology preferred - board eligibility considered.
6-8 years of experience in clinical practice, academia, research, or industry is an advantage.
Excellent communication and presentation skills.
Ability to work collaboratively in cross-functional teams.
Willingness to travel 60-70% of the time, including some weekends.
Why Zoetis?
Innovative Environment: Be part of a company that values innovation and is at the forefront of veterinary medicine. Committed to Science - Committed to Dermatology.
Professional Growth: Access continuous learning opportunities and professional development programs.
Collaborative Culture: Work in a supportive, team-oriented environment where we believe our colleagues make the difference.
The US base salary range for this full-time position is $167,000-205,000. Our salary ranges are
determined by role, level, and location. The range displayed on each job posting reflects the base pay target range
for new hire salaries for the position. Within the range, individual pay is determined by work location and additional
factors, including job-related skills, experience, and relevant education or training.
[This position is also eligible for short-term incentive compensation
[This position is also eligible for long-term incentives
In addition to compensation, Zoetis offers a comprehensive benefits package that supports the physical, emotional
and financial wellbeing of our colleagues and their families including healthcare and insurance benefits beginning
on day one, a 401K plan with a match and profit-sharing contribution from Zoetis, and 4 weeks of vacation.
Visit zoetisbenefits.com to learn more.
Full time RegularColleague
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.
$167k-205k yearly Auto-Apply 6d ago
SR AD, GFE
Boehringer Ingelheim 4.6
Barceloneta, PR jobs
As an integral member of the Barceloneta Site Leadership team, the Head of GFE Barceloneta has end to end accountability for the Global Facilities & Engineering (GFE) functions. This role is responsible for executing global strategy and regional action plans for Barceloneta, and for managing / optimizing site performance.
The Local Head of GFE Barceloneta ensures:
+ Pursuit of GFE / Business Unit (BU) strategy from a Site Services perspective, incl. adherence to global standards for GFE and local regulations
+ Tactical leadership of capital investment budgeting, asset management and engineering project execution
+ Execution of fast, agile and high-quality Site Services following common standards
+ Reporting to Head of GFE AH Networks and Site Hed Barceloneta on local & site-specific regulations compliance, & actions to protect BI's reputation
+ Proactively managing the organizational risks on site
+ Safety and security of BI employees and assets
+ Leadership, people development and employee reviews
**Duties & Responsibilities**
+ Lead, oversee and direct these functions: Engineering (including Process Engineering, Automation, Maintenance & Digitalization, Capital Projects), Real Estate & Facility Management, Environmental, Health Safety, Sustainability and Security.
+ Accountability for budget oversight, capital project management, sustainability targets, and facility, plant, utility, environmental & security operations.
+ Aggregates & approves budget proposals from site GFE functions & communicates to the regional level.
+ Implement priorities and targets as defined by Global/Regional Head of GFE and Head of BU GE. Ensures local targets are coherent for GFE functions (no conflicting targets).
+ Safeguards effective solution delivery by aggregating and reporting GFE function performance, quality and compliance to the regional / global level.
+ Develop and execute key technical engineering strategies within production areas to improve critical process efficiency / performance. Ensure process improvement projects are incorporated into strategic CapEx and OpEx plans / budgets.
+ Develop & effectively manage CapEx Project execution based on site, regional & global BU strategy. Ensure CapEx management meets Corp. standards & procedures. Collaborate with GFE Project Management for Strategic Projects (over 50M EUR)
+ Oversee execution of selected services on site according to defined standards & performance levels. Ensure best practice sharing across GFE functions (if applicable).
+ Review & align local or BU-specific adaptations of global concepts, standards, and processes with Regional Head of GFE / Head of BU GE when required.
+ Accountable to ensure all regulatory and (site-specific) legal requirements are being followed.
+ Ensure safety and security of BI assets and employees as well sustainability of services and facilities.
+ Oversees Talent Management and employee lifecycle for GFE functions on site level.
+ Proven track-record in successfully executed CapEx projects
**Requirements**
+ University degree in the respective field of responsibility
+ 5-10 years of experience on a site in a leading position
+ 3-5 years of experience in one or more GFE functions present at the site
+ Proven track record in site operations
+ Routine exposure to inspections / audits (agencies, customers, suppliers, etc.) with successful outcomes
+ Proven team & individual performance management, including coaching and development, leading to consistent delivery of targeted results
+ Visionary leadership competencies & passionate team player (also in virtual setting)
+ Service orientation and customer focus
+ Multi cultural awareness and understanding
+ Internal / external networking across functions and different executive levels
**Eligibility Requirements:**
+ Must be legally authorized to work in the United States without restriction.
+ Must be willing to take a drug test and post-offer physical (if required).
+ Must be 18 years of age or older.
All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.
$97k-117k yearly est. 40d ago
Senior Talent Engagement Specialist
Niowave 3.5
Lansing, MI jobs
Summary/Objective
Under the direction of the Chief People Officer, the Talent Engagement Specialist will be responsible for full cycle recruitment activities that meet/exceed established objectives. This position plays a critical role in ensuring that the organization meets its goal of quickly finding and placing high quality talent. Serving as the initial contact representative and the face of the organization, the TES is a people person - you love to start new conversations, network, attend events and meet new people. Juggling multiple projects and working with different teams, you stay detail focused with the end goal in mind. Words that describe you are outgoing, flexible, motivated and creative. You are technologically savvy and are a fast learner.
Essential Functions
Collaborates with departmental managers to understand skills and competencies required for job openings, develops, and maintains s, recruits, schedules interviews, and facilitates the hiring of qualified job applicants for open positions; determine selection criteria, candidate screening, interviewing, wage negotiation, hiring and onboarding.
Manage full-cycle technical recruiting process for assigned professional teams (including but not limited to Chemistry, Nuclear Engineering, Manufacturing, Business Support Services, Accelerator and Electrical Engineering).
Manages the recruitment module.; utilize innovative recruiting methods including social media sites, networking events, building partnerships, etc. to find qualified candidates.
Actively participate in networking groups and other business and community programs to increase skill knowledge of current recruiting practices.
Work closely with Hiring Managers to maximize effectiveness of recruiting process and project future hiring requirements.
Understand business strategy and provide innovative and creative recruitment solutions in response to hiring needs.
Brand and market the culture and commitment to the community through relationship-building with community partners, including campus relationships.
Contribute to recruiting efforts by attending early talent career fairs, manufacturing job fairs and community events.
Competencies
Business Acumen; Analytical Skills.
HR body of knowledge.
Consultation; Critical Evaluation.
Global & Cultural Awareness.
Relationship Management.
Ethical Practice.
Excellent interpersonal, written, and oral communication skills.
Able to prioritize and execute tasks in a high-pressure environment.
Expertly performs in a team-oriented, collaborative environment.
Excellent communication and interpersonal skills - you know how to develop & maintain strong relationships with all levels/teams of the organization.
Understand how to integrate into a new team/organization - appreciate the history of current state, know how and when to make suggestions, as well as using just the right pace to reach the improved future state.
Understand your own communication and learning styles, assess others styles, and are able to find the right path to connect the two.
Exceptional technology skills - you find working with any software very comfortable and you easily adapt to new products and highly efficient with MS Office products.
Highly values integrity, professionalism, and confidentiality.
Embraces the Niowave Values of Teamwork, Courage, Integrity, and Upright Zeal.
Required Education and Experience
Four-year degree in Human Resources, Business or related field or equivalent.
Minimum of five years technical and/or professional candidate recruiting experience.
Familiarity with HR hiring plan development & staffing processes.
An understanding and working knowledge of employment law, applicant tracking systems, internet recruiting, advertising, interviewing, and staffing assessment.
Ability to obtain a working knowledge of the Niowave culture and specific position requirements.
Proficiency in Microsoft Office.
Preferred Education and Experience
Four-year degree in Human Resources, Business or related field.
Experience working in a manufacturing or pharmaceutical organization.
Work Environment
This job operates in a professional office environment. This role routinely uses standard office equipment.
Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; climb stairs; talk or hear. The employee must occasionally lift or move office products and supplies, up to 20 pounds.
Position Type/Expected Hours of Work
Full-time position (or as assigned).
Company's standard operating hours are Monday thru Friday 6a - 6p with production related activities requiring 24/7/365 shifts. This position will have regular working hours during M - F with an expectation of adjusting to meet with managers and candidates outside of the standards operating hours as needed.
Niowave has multiple locations within the Lansing area. Travel between locations is expected in the role.
Other duties
Please note 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.
$72k-111k yearly est. 60d+ ago
Senior Training Specialist
Amneal Pharmaceuticals 4.6
Piscataway, NJ jobs
The Senior Training Specialist plays a vital role in fostering a culture of learning and compliance at Amneal. This position ensures the accuracy and security of training records while driving the development of effective training programs that empower employees and contractors to succeed. Working closely with cross-functional teams the Senior Training Specialist helps translate regulatory requirements into practical, engaging learning experiences. Beyond maintaining curricula and supporting audits, this role is about inspiring confidence, building knowledge, and strengthening quality standards across the organization. As a key contributor to Amneal's mission, the Senior Training Specialist not only supports compliance but also champions professional growth, making training a meaningful part of every employee's journey.
Essential Functions:
Evaluate change controls, CAPAs, and investigations to identify training needs.
Develop training plans for new or revised SOPs; ensure SOPs are effective only after required training.
Prepare, issue, and monitor training materials and curricula; maintain supplies and equipment.
Deliver cGMP training (New Hire, Annual, classroom, and online) using Global Quality-approved materials.
Collaborate with functional heads and cross-functional teams to update and maintain curricula.
Create training modules using GMP guidance and deliver as required.
Support the Quality Unit with training metrics, including preparation for Quality Review Board (QRB).
Serve as key auditee during internal, customer, and regulatory inspections; provide requested documentation.
Oversee SETE training staff for data entry and audit support.
Coordinate with IT on LMS implementation, data migration, and management.
Act as process owner for Amneal's learning management system (LMS) and support Amneal University program.
Additional Responsibilities:
Follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seeks guidance as necessary.
Actively supports and participates in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Injury and Illness Prevention Program (I2P2).
Carries out all responsibilities in an honest, ethical, and professional manner.
Handles various other duties as delegated by direct supervisor/management.
Education:
Bachelors Degree (BA/BS) - Required
Experience:
3 years or more of experience in GxP training, Quality Assurance, or related pharmaceutical/biotech roles
Skills:
Advanced proficiency in Microsoft Office Suite. Office 365 preferred experience. - Proficient
Knowledge of compliance and audit requirements. - Proficient
Ability to conduct research and apply relevant information to training programs that support organizational effectiveness. - Proficient
Must be able to work in a fast-paced environment and thrive with ambiguity. - Proficient
Ability to meet tight deadlines and effectively prioritize and juggle multiple concurrent projects - Proficient
Must have a strong work ethic and a positive attitude. - Proficient
Excellent communication skills, both verbal and written. - Proficient
Results-driven achiever with exemplary planning and organizational skills, along with a high attention to detail. - Proficient
Strong assessment, analytical, critical thinking, and problem-solving skills. - Proficient
Innovative problem-solver who can generate workable solutions and address needs. - Proficient
Specialized Knowledge:
Comprehensive knowledge of Microsoft Office programs Experience with an e-Learning computer program a plus
The base salary for this position ranges from $100,000 to $115,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills.
At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.
$100k-115k yearly Auto-Apply 4d ago
Senior Training Specialist
Amneal Pharmaceuticals, Inc. 4.6
Piscataway, NJ jobs
The Senior Training Specialist plays a vital role in fostering a culture of learning and compliance at Amneal. This position ensures the accuracy and security of training records while driving the development of effective training programs that empower employees and contractors to succeed. Working closely with cross-functional teams the Senior Training Specialist helps translate regulatory requirements into practical, engaging learning experiences. Beyond maintaining curricula and supporting audits, this role is about inspiring confidence, building knowledge, and strengthening quality standards across the organization. As a key contributor to Amneal's mission, the Senior Training Specialist not only supports compliance but also champions professional growth, making training a meaningful part of every employee's journey.
Essential Functions:
* Evaluate change controls, CAPAs, and investigations to identify training needs.
* Develop training plans for new or revised SOPs; ensure SOPs are effective only after required training.
* Prepare, issue, and monitor training materials and curricula; maintain supplies and equipment.
* Deliver cGMP training (New Hire, Annual, classroom, and online) using Global Quality-approved materials.
* Collaborate with functional heads and cross-functional teams to update and maintain curricula.
* Create training modules using GMP guidance and deliver as required.
* Support the Quality Unit with training metrics, including preparation for Quality Review Board (QRB).
* Serve as key auditee during internal, customer, and regulatory inspections; provide requested documentation.
* Oversee SETE training staff for data entry and audit support.
* Coordinate with IT on LMS implementation, data migration, and management.
* Act as process owner for Amneal's learning management system (LMS) and support Amneal University program.
Additional Responsibilities:
* Follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seeks guidance as necessary.
* Actively supports and participates in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Injury and Illness Prevention Program (I2P2).
* Carries out all responsibilities in an honest, ethical, and professional manner.
* Handles various other duties as delegated by direct supervisor/management.
$75k-107k yearly est. Auto-Apply 4d ago
Senior Training Specialist
Amneal Pharmaceuticals 4.6
Brookhaven, NY jobs
The Senior Training Specialist plays a vital role in fostering a culture of learning and compliance at Amneal. This position ensures the accuracy and security of training records while driving the development of effective training programs that empower employees and contractors to succeed. Working closely with cross-functional teams, the Senior Training Specialist helps translate regulatory requirements into practical, engaging learning experiences. Beyond maintaining curricula and supporting audits, this role is about inspiring confidence, building knowledge, and strengthening quality standards across the organization. As a key contributor to Amneal's mission, the Senior Training Specialist not only supports compliance but also champions professional growth, making training a meaningful part of every employee's journey.
Schedule:
1st Shift 9am - 5:30pm Monday to Friday
Essential Functions
Evaluate change controls, CAPAs, and investigations to identify training needs.
Develop training plans for new or revised SOPs; ensure SOPs are effective only after required training.
Prepare, issue, and monitor training materials and curricula; maintain supplies and equipment.
Deliver cGMP training (New Hire, Annual, classroom, and online) using Global Quality-approved materials.
Collaborate with functional heads and cross-functional teams to update and maintain curricula.
Create training modules using GMP guidance and deliver as required.
Support the Quality Unit with training metrics, including preparation for Quality Review Board (QRB).
Serve as key auditee during internal, customer, and regulatory inspections; provide requested documentation.
Oversee SETE training staff for data entry and audit support.
Coordinate with IT on LMS implementation, data migration, and management.
Act as process owner for Amneal's learning management system (LMS) and support Amneal University program.
Additional Responsibilities:
Follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seeks guidance as necessary.
Actively supports and participates in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Injury and Illness Prevention Program (I2P2).
Carries out all responsibilities in an honest, ethical, and professional manner.
Handles various other duties as delegated by direct supervisor/management.
Education:
Bachelors Degree (BA/BS) - Required
Experience:
3 years or more of experience in GxP training, Quality Assurance, or related pharmaceutical/biotech roles
Skills:
Advanced proficiency in Microsoft Office Suite. Office 365 experience preferred. - Proficient
Knowledge of compliance and audit requirements. - Proficient
Ability to conduct research and apply relevant information to training programs that support organizational effectiveness. - Proficient
Must be able to work in a fast-paced environment and thrive with ambiguity. - Proficient
Ability to meet tight deadlines and effectively prioritize and juggle multiple concurrent projects - Proficient
Must have a strong work ethic and a positive attitude. - Proficient
Excellent communication skills, both verbal and written. - Proficient
Results-driven achiever with exemplary planning and organizational skills, along with a high attention to detail. - Proficient
Strong assessment, analytical, critical thinking, and problem-solving skills. - Proficient
Innovative problem-solver who can generate workable solutions and address needs. - Proficient
Specialized Knowledge:
Comprehensive knowledge of Microsoft Office programs Experience with an e-Learning computer program a plus
The base salary for this position ranges from $100,000 to $115,000 per year. Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life's many other commitments and opportunities.
$100k-115k yearly Auto-Apply 3d ago
Senior Training Specialist
Amneal Pharmaceuticals, Inc. 4.6
Brookhaven, NY jobs
The Senior Training Specialist plays a vital role in fostering a culture of learning and compliance at Amneal. This position ensures the accuracy and security of training records while driving the development of effective training programs that empower employees and contractors to succeed. Working closely with cross-functional teams, the Senior Training Specialist helps translate regulatory requirements into practical, engaging learning experiences. Beyond maintaining curricula and supporting audits, this role is about inspiring confidence, building knowledge, and strengthening quality standards across the organization. As a key contributor to Amneal's mission, the Senior Training Specialist not only supports compliance but also champions professional growth, making training a meaningful part of every employee's journey.
Schedule:
1st Shift 9am - 5:30pm Monday to Friday
Essential Functions
* Evaluate change controls, CAPAs, and investigations to identify training needs.
* Develop training plans for new or revised SOPs; ensure SOPs are effective only after required training.
* Prepare, issue, and monitor training materials and curricula; maintain supplies and equipment.
* Deliver cGMP training (New Hire, Annual, classroom, and online) using Global Quality-approved materials.
* Collaborate with functional heads and cross-functional teams to update and maintain curricula.
* Create training modules using GMP guidance and deliver as required.
* Support the Quality Unit with training metrics, including preparation for Quality Review Board (QRB).
* Serve as key auditee during internal, customer, and regulatory inspections; provide requested documentation.
* Oversee SETE training staff for data entry and audit support.
* Coordinate with IT on LMS implementation, data migration, and management.
* Act as process owner for Amneal's learning management system (LMS) and support Amneal University program.
Additional Responsibilities:
* Follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seeks guidance as necessary.
* Actively supports and participates in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Injury and Illness Prevention Program (I2P2).
* Carries out all responsibilities in an honest, ethical, and professional manner.
* Handles various other duties as delegated by direct supervisor/management.
$63k-89k yearly est. Auto-Apply 4d ago
Senior Training Specialist
Amneal Pharmaceuticals 4.6
Branchburg, NJ jobs
The Senior Training Specialist plays a vital role in fostering a culture of learning and compliance at Amneal. This position ensures the accuracy and security of training records while driving the development of effective training programs that empower employees and contractors to succeed. Working closely with cross-functional teams, the Senior Training Specialist helps translate regulatory requirements into practical, engaging learning experiences. Beyond maintaining curricula and supporting audits, this role is about inspiring confidence, building knowledge, and strengthening quality standards across the organization. As a key contributor to Amneal's mission, the Senior Training Specialist not only supports compliance but also champions professional growth, making training a meaningful part of every employee's journey.
Essential Functions:
Evaluate change controls, CAPAs, and investigations to identify training needs.
Develop training plans for new or revised SOPs; ensure SOPs are effective only after required training.
Prepare, issue, and monitor training materials and curricula; maintain supplies and equipment.
Deliver cGMP training (New Hire, Annual, classroom, and online) using Global Quality-approved materials.
Collaborate with functional heads and cross-functional teams to update and maintain curricula.
Create training modules using GMP guidance and deliver as required.
Support the Quality Unit with training metrics, including preparation for Quality Review Board (QRB).
Serve as key auditee during internal, customer, and regulatory inspections; provide requested documentation.
Oversee SETE training staff for data entry and audit support.
Coordinate with IT on LMS implementation, data migration, and management.
Act as process owner for Amneal's learning management system (LMS) and support Amneal University program.
Additional Responsibilities:
Follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seeks guidance as necessary.
Actively supports and participates in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Injury and Illness Prevention Program (I2P2).
Carries out all responsibilities in an honest, ethical, and professional manner.
Handles various other duties as delegated by direct supervisor/management.
Education:
Bachelors Degree (BA/BS) - Required
Experience:
3 years or more in experience in GxP training, Quality Assurance, or related pharmaceutical/biotech roles
Skills:
Advanced proficiency in Microsoft Office Suite. Office 365 experience preferred. - Proficient
Knowledge of compliance and audit requirements. - Proficient
Ability to conduct research and apply relevant information to training programs that support organizational effectiveness. - Proficient
Must be able to work in a fast-paced environment and thrive with ambiguity. - Proficient
Ability to meet tight deadlines and effectively prioritize and juggle multiple concurrent projects - Proficient
Must have a strong work ethic and a positive attitude. - Proficient
Excellent communication skills, both verbal and written. - Proficient
Results-driven achiever with exemplary planning and organizational skills, along with a high attention to detail. - Proficient
Strong assessment, analytical, critical thinking, and problem-solving skills. - Proficient
Innovative problem-solver who can generate workable solutions and address needs. - Proficient
Specialized Knowledge:
Comprehensive knowledge of Microsoft Office programs Experience with an e-Learning computer program a plus
The base salary for this position ranges from $100,000 to $115,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills.
At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.
$100k-115k yearly Auto-Apply 4d ago
Senior Training Specialist
Amneal 4.6
Somerville, NJ jobs
The Senior Training Specialist plays a vital role in fostering a culture of learning and compliance at Amneal. This position ensures the accuracy and security of training records while driving the development of effective training programs that empower employees and contractors to succeed. Working closely with cross-functional teams, the Senior Training Specialist helps translate regulatory requirements into practical, engaging learning experiences. Beyond maintaining curricula and supporting audits, this role is about inspiring confidence, building knowledge, and strengthening quality standards across the organization. As a key contributor to Amneal's mission, the Senior Training Specialist not only supports compliance but also champions professional growth, making training a meaningful part of every employee's journey.
Essential Functions:
Evaluate change controls, CAPAs, and investigations to identify training needs.
Develop training plans for new or revised SOPs; ensure SOPs are effective only after required training.
Prepare, issue, and monitor training materials and curricula; maintain supplies and equipment.
Deliver cGMP training (New Hire, Annual, classroom, and online) using Global Quality-approved materials.
Collaborate with functional heads and cross-functional teams to update and maintain curricula.
Create training modules using GMP guidance and deliver as required.
Support the Quality Unit with training metrics, including preparation for Quality Review Board (QRB).
Serve as key auditee during internal, customer, and regulatory inspections; provide requested documentation.
Oversee SETE training staff for data entry and audit support.
Coordinate with IT on LMS implementation, data migration, and management.
Act as process owner for Amneal's learning management system (LMS) and support Amneal University program.
Additional Responsibilities:
Follows all organizational systems, programs, training, policies, and procedures as required and complies with relevant legal mandates. Seeks guidance as necessary.
Actively supports and participates in the safety program, both for self-protection and the protection of other employees, by reading and abiding by all requirements in the Injury and Illness Prevention Program (I2P2).
Carries out all responsibilities in an honest, ethical, and professional manner.
Handles various other duties as delegated by direct supervisor/management.
Qualifications
Education:
Bachelors Degree (BA/BS) - Required
Experience:
3 years or more in experience in GxP training, Quality Assurance, or related pharmaceutical/biotech roles
Skills:
Advanced proficiency in Microsoft Office Suite. Office 365 experience preferred. - Proficient
Knowledge of compliance and audit requirements. - Proficient
Ability to conduct research and apply relevant information to training programs that support organizational effectiveness. - Proficient
Must be able to work in a fast-paced environment and thrive with ambiguity. - Proficient
Ability to meet tight deadlines and effectively prioritize and juggle multiple concurrent projects - Proficient
Must have a strong work ethic and a positive attitude. - Proficient
Excellent communication skills, both verbal and written. - Proficient
Results-driven achiever with exemplary planning and organizational skills, along with a high attention to detail. - Proficient
Strong assessment, analytical, critical thinking, and problem-solving skills. - Proficient
Innovative problem-solver who can generate workable solutions and address needs. - Proficient
Specialized Knowledge:
Comprehensive knowledge of Microsoft Office programs Experience with an e-Learning computer program a plus
The base salary for this position ranges from $100,000 to $115,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills.
At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.
$100k-115k yearly Auto-Apply 4d ago
Training Specialist
Trialcard 4.6
Morrisville, NC jobs
Remote is Role, but preferably looking for this person to reside in North Carolina.
Valeris is an integrated life sciences commercialization partner that provides comprehensive solutions that span the entire healthcare value chain. Backed by proven industry expertise and results-driven technology, Valeris helps navigate the complex life sciences marketplace by providing commercialization solutions to accelerate value and enhance patient lives.
Valeris fosters a culture that encourages individuality and provides opportunities for creativity, growth, and success while fostering a team environment. We are a diversity-driven organization with an inclusive approach to delivering patient-centric solutions that eliminate barriers for patients and increase access to life-altering medications.
The Training Specialist position is responsible for helping our new hires gain the skills and acumen needed to succeed in their new positions. They will facilitate refresher and skills training to ensure current employees excel in their current roles. Using principles of adult learning, the Training Specialist will develop instructional materials and deliver training programs for the Valeris team. The position will modify instructional materials in response to evaluations from learners and organizational changes. This role interacts with individuals from multiple departments and plays a key part in building the Learning and Development function.
Responsibilities
Design and develop training materials for new programs and maintain existing materials (e.g., instructor-led training, eLearning modules, job aids, activities, and desk drops).
Lead new hire training sessions covering specified areas such as computer and platform usage, new hire onboarding, refresher training, and system or process upgrade training.
Deliver required compliance training for new hires prior to their active support of any assigned program.
Measure trainee progress to evaluate training effectiveness and determine readiness for trainees to perform in their assigned roles.
Document areas of concern for trainees and review findings with Program Leadership.
Collaborate with Program Leadership to remain informed of changes in policies, procedures, regulations, and technologies.
Update the SharePoint site to ensure content is current, accurate, grammatically correct, and user-friendly.
Maintain and promote a positive learning environment in all training settings.
Adhere to all training deadlines and corporate policies related to access and handling of confidential data.
Ensure all SOPs are followed consistently across training delivery and documentation.
Perform additional tasks or projects as assigned.
Qualifications
Minimum Qualifications
College degree in Communication, Education, or a related field and/or equivalent experience in training
Experience designing training materials and delivering training in a corporate setting
Experience managing and facilitating meetings with key stakeholders
Excellent interpersonal skills, including the ability to quickly develop strong working relationships
Excellent verbal and written communication skills
Ability to work in a fast-paced, ever-changing environment
Proven ability to mentor others to ensure their success
Preferred Qualifications
Degree in a related discipline such as Instructional Design, Organizational Psychology, Adult Education, etc.
At least 2 years of experience working in the pharmaceutical industry and at least 1 year of training experience
$45k-68k yearly est. Auto-Apply 29d ago
Production Training Specialist
Jost Chemical Co 4.2
Saint Louis, MO jobs
Are you ready to embark on a career where innovation meets excellence? At Jost Chemical Company, we're on a mission to push the boundaries of chemical manufacturing, delivering high-quality products that make a positive impact on global industries. If you're passionate about chemistry, dedicated to precision, and eager to contribute to a company that values both innovation and integrity, explore our exciting job opportunities. Join us in shaping the future of chemical manufacturing at Jost Chemical Company, where your career is more than just a job - it's a journey of growth and achievement.
Then, this position is right for you!
Founded in 1985, Jost Chemical is a global leader in the manufacture of high purity mineral salts for the nutritional, pharmaceutical and specialty markets. Expansion, growth of capabilities, and investment in people, lab and production equipment have been a part of Jost's company culture for 40 years. To learn more about Jost Chemical please visit ********************
Our offer:
* Shift Differential
* Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance first of the month following 60 days.
* 401k plan which includes safe-harbor contribution and discretionary match.
* Paid Time Off (PTO) Employees eligible first day of employment.
* 9 Company Paid Holidays (72 hours) each year.
* Uniforms Provided
* Foot Protection- annual allowance for all laboratory, maintenance and production employees.
* 24-hour access to our free, on-site fitness center.
* We provide Individual development, on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at work.
Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status. We are committed to recruiting and retaining the best talent in the chemical manufacturing industry.
Position Summary
The Production Training Specialist works under the direct supervision of the Production Training Supervisor in a GMP-regulated manufacturing environment operating under Q7A standards. This role supports the development, coordination, and delivery of training programs to ensure employee safety, GMP compliance, and operational excellence across Packaging and Operations.
In addition to training and documentation responsibilities, this role may support production activities as a Packager or Operator when needed.
Key Responsibilities
* Support and enhance site safety through effective training and awareness programs.
* Perform and coordinate introductory and onboarding training for new employees.
* Assist in the review, creation, and updating of SOPs across all departments.
* Identify training gaps and propose corrective actions for operational staff.
* Organize and maintain GMP and regulatory training documentation, including safety, GMP, and operator skill records.
* Collaborate with Quality and EHS teams to support employee awareness and compliance initiatives.
* Develop training programs to transition existing employees into new roles.
* Develop, implement, and maintain training programs and curricula across the organization.
* Create innovative training methods to reduce errors, improve productivity, and strengthen safety culture.
* Develop and maintain training evaluation tools to measure effectiveness.
* Maintain and optimize training systems; troubleshoot training-related issues.
* Work closely with on-the-job trainers to support employee development.
* Assist with administration and recordkeeping of training for Packaging and Operations departments.
* Participate in special projects and support production operations as needed.
Qualifications
Education & Experience
* Post-secondary education in an administrative or technical field preferred (technical background desirable).
* Minimum of 3 years of experience in chemical manufacturing operations and/or packaging.
Knowledge
* Safety, health, and environmental regulations, policies, and procedures.
* Training needs assessment, adult learning principles, and course development.
* GMP requirements and regulated manufacturing environments.
* Microsoft Office applications.
* Mathematics and English comprehension.
Skills
* Strong oral and written communication skills across all organizational levels.
* Ability to troubleshoot operational and training issues.
* Understanding of production operations, process control, and monitoring.
* Strong organizational and documentation skills.
Ability to:
* Follow established policies and procedures
* Develop and interpret training documents
* Present information in professional and knowledgeable manner
* Adapt to rapidly changing priorities based on business needs
* Work off-shift/weekends as needed
* Work in extreme cold and hot (120 F) environment
* Ability to lift 55 pounds and drive fork truck in safe and efficient manner
* Operate and maintain chemical processing equipment
* Pass pre-employment physical with drug screen and physical capabilities test
Monday - Friday - 6:30 - 3pm