Material Handler - TEMP
Noven Pharmaceuticals job in Miami, FL
Under supervision comply with cGMP, current SOPs, safety and environmental guidelines. Perform warehousing duties and staging of raw materials for manufacturing operations. Prepare shipments of finished product and miscellaneous items for outside processing. Perform inventory, cycle count, and receiving transactions using Noven's integrated systems (MRP / DSI) to ensure inventory and location accuracy. Assist with the delivery of small packages and mail delivery as needed. Work as an effective team member, to ensure that the department's quality and performance expectations are met. Forklift operation is required.
Responsibilities
Receive materials by unloading trucks, verifying that quantities and match materials received with the shipping documentation; perform electronic receiving transactions using DSI.
Maintain location accuracy, consolidating locations as needed, identify / report deterioration and/or damage conditions of stored materials.
Maintain inventory accuracy by ensuring that all inventory moves are posted on a timely basis by using Noven's integrated system (MRP / DSI)
Perform inventory cycle counts and report inventory errors or discrepancies to Inventory Control.
Operate heavy equipment (Forklift / Truck) to support the manufacturing operations and request made by internal Noven customers.
Dispense materials for manufacturing work orders, per pick lists and SOP requirements.
Receive returns from manufacturing; verify the quantities and lot number against return documentation, process return per SOP requirements.
Check Temperature Chart Recorders daily per current SOP.
Assist with the distribution of mail, small packages, and other items between facilities, as required; including clerical and physical activities.
Comply with cGMP, EHS guidelines, and all SOPs assigned to the position. Maintain warehouse housekeeping in excellent conditions.
Perform special duties or projects as necessary.
Qualifications
Competencies:
Education / Experience:
High School Diploma or GED required. 1 - 3 years of professional experience preferably in a GMP manufacturing environment. Good verbal and written communication skills; organized and able to efficiently follow directions under supervision. Must have a basic computer skill set; including knowledge of MS Word, Excel, and e-mail. Licensed forklift operator preferred. Must have a valid driver's license; with the ability to operate an automobile, van, or truck. Have an internal and external customer orientation; willingness to learn and effectively practice new methodologies and technologies.
Judgment / Decision Making:
Duties performed independently toward general results; modification and interpretation of guidelines sometimes required.
Work Environment:
Warehouse environment with exposure to chemicals, fumes, high places, and moving parts. Nature of duties performed could result in injuries due to carelessness.
Physical Demands:
Regularly lift and carry objects weighing up to 50 pounds. Individual is required to stand for more than two hours at a time, while stooping and bending. Visual acuity to proofread documents.
Auto-ApplyCalibration Technician
Noven Pharmaceuticals job in Miami, FL
Overview Seeking Metrology/Calibration Technician (entry level) to calibrate and repair test instruments in accordance with precision standards and procedures. The ideal applicant is familiar with various test and measurement processes, self-motivated, a team player, and has a strong commitment to continuous improvement. Responsibilities
Perform calibration, testing, troubleshooting, and repairs on a wide range of measuring and test equipment.
Complete required documentation to certify the verification and calibration of measuring and test equipment.
Set up standard and special purpose laboratory equipment to test, evaluate, and calibrate other instruments and test equipment.
Manage time to achieve maximum efficiency.
Perform routine equipment maintenance.
Calibrate equipment to industry standards.
Troubleshoot equipment failures.
Conduct equipment repairs.
Respond to departmental queries.
Suggest equipment upgrades.
Maintain calibration equipment and supplies.
Work with outside vendors to accomplish calibration/maintenance tasks.
Other duties as directed by supervisor
Qualifications
Competencies
Education / Experience:
High school diploma
1+ years of instrumentation experience preferred.
Experience in various fields of calibration, preferably pharmaceutical.
Knowledgeable in cGMP requirements.
Ability to identify resources when necessary.
Must be computer literate with knowledge of office application software (Microsoft Word, Excel, PowerPoint, ACCESS, and Outlook).
Excellent communication skills, both written and verbal
Judgment / Decision Making:
Under general supervision, exercises some judgement in accordance with well-defined policies, procedures and techniques.
Moderately complex work performed within established practices and procedures requiring original thinking.
Effectively identifies problems as they occur and takes appropriate steps to solve straight-forward problems.
Works on assignments that may be complex in nature where considerable judgment and initiative are required in resolving problems and making recommendations.
May determine methods and procedures on new assignments and may provide guidance to other non-exempt personnel
Work Environment:
While performing the duties of this Job, the employee is regularly exposed to moving mechanical parts. The noise level in the work environment is usually moderate. May be required to work in areas where high noise hazards prevail. May be exposed to fumes or airborne particles.
Physical Demands:
Often required to stand for up to an hour at a time with stooping and bending.
Required to walk, sit, and use fingers and hands, handle or feel tools or controls, reach with hands and arms, balance, stoop, crouch, bend, talk and hear.
Must lift and/or move up to 50 pounds.
Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, and depth perception
Auto-ApplyPsychiatry Account Manager - South Orlando / Melbourne, FL
Orlando, FL job
Territory: South Orlando / Melbourne, FL - Psychiatry
Target cities for territory are southern Orlando, Kissimmee, or St Cloud - will consider candidates who live within 40 miles of territory boundaries with access to a major airport. Territory boundaries include: Kissimmee, St. Cloud, Winterhaven, North to Southern Orlando, Rockledge, South to Palm Bay, and Melbourne.
SUMMARY:
Are you a results-driven biopharmaceutical sales professional looking to be part of an organization that values being curious, adaptable and accountable? Lundbeck is a global biopharmaceutical company focusing exclusively on brain health. With more than 70 years of experience in neuroscience, we are committed to improving the lives of people with neurological and psychiatric diseases. Lundbeck employees are inspired and driven by our purpose to advance brain health and transform lives. Join us on our journey of growth!
As a Psychiatry Account Manager, you lead the promotion of our psychiatry portfolio, executing sales and marketing strategies with comprehensive clinical knowledge to drive sales performance. Our Account Managers are adept at executing against the toughest commercialization challenges in today's rapidly changing environment and must demonstrate strong capability in the following areas:
ESSENTIAL FUNCTIONS:
Business Planning & Account Leadership - Ability to use digital tools and apply data-based insights to create opportunities, develop strategy & tactics, allocate resources to enhance sales execution, monitor progress and adjust direction to maximize sales performance.
Selling - Deliver messages in a clear and compelling way to customers, effectively probe customer needs to handle objections, and close every call with a commitment to action to drive changes in behavior.
Customer Development - Build and maintain productive internal and external relationships based on customer needs and organizational goals, incorporating “total office” account management.
Local Market & Therapeutic Area Expertise - Gather and validate key trends and dynamics in the market, map account linkages, and apply comprehensive therapeutic knowledge to uncover and prioritize unique opportunities.
Reimbursement - Consistently demonstrate the ability to stay informed on reimbursement dynamics, anticipate and effectively address payer access issues (IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources.
Pharmaceutical Environment/Compliance - Ability to apply knowledge of pharmaceutical and regulatory environment, including accountability and adherence to Lundbeck policies and procedures and FDA regulations regarding the promotion of pharmaceutical and medical products.
REQUIRED EDUCATION, EXPERIENCE and SKILLS:
Bachelor of Arts or Bachelor of Sciences degree from an accredited college or university
2+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience
Must demonstrate the intellectual capacity to score highly on disease and product training exams, including being certified on product knowledge annually
Self-starter, with a strong work ethic and outstanding communication skills
Must be computer literate with proficiency in Microsoft Office software
Must live within 40 miles of territory boundaries
Driving is an essential duty of this job; must have a valid driver's license with a safe driving record that meets company requirements
Meeting and complying with reasonable industry-standard credentialing requirements of healthcare providers / customer facilities is required for continued employment with Lundbeck
PREFERRED EDUCATION, EXPERIENCE AND SKILLS:
Previous experience within a specialty product sales force
Prior experience promoting and detailing products specific to CNS/neuroscience including: depression, schizophrenia and bipolar disorder
Documented successful sales performance
Ownership and accountability for the development and execution of fully integrated account plans
Strong analytical background, and experience using sales data reporting tools to identify trends
Experience in product launches
Previous experience working with alliance partners (i.e., co-promotions)
Strong leadership through participation in committees, job rotations, panels and related activities
TRAVEL:
Willingness/Ability to travel up to 30% - 40% domestically to (a) regularly meet/interact with customer base and internal personnel within assigned territory; and (b) typically attend 4-8 internal/external conferences and meetings spanning locations within the United States. Travel must be able to be completed in a timely manner.
The range displayed is a national range, and if selected for this role, may vary based on various factors such as the candidate's geographical location, qualifications, skills, competencies, and proficiency for the role. Salary Pay Range: $117,000 - $137,000 and eligibility for a sales incentive target of $39,000. Benefits for this position include flexible paid time off (PTO), health benefits to include Medical, Dental and Vision, company match 401k and company car. Additional benefits information can be found on our career site. Applications accepted on an ongoing basis.
Why Lundbeck
Lundbeck offers a robust and comprehensive benefits package to help employees live well and protect their health, family, and everyday life. Information regarding our benefit offering can be found on the U.S. career site.
Lundbeck is committed to working with and providing reasonable accommodations to disabled veterans and other individuals with disabilities during our employment application process. If, because of a disability, you need a reasonable accommodation for any part of the application process, please visit the U.S. career site.
Lundbeck is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, and any other characteristic protected by law, rule, or regulation. Lundbeck participates in E-Verify.
Multi-Specialty Account Manager - Naples, FL
Naples, FL job
Territory: Naples, FL - Multi-Specialty
Target city for territory is Naples - will consider candidates who live within 40 miles of territory boundaries with access to a major airport. Territory boundaries include: Sarasota, Arcadia, Marco Island, Clewiston, Immokalee, Venice, Fort Myers Beach.
SUMMARY:
Are you a results-driven biopharmaceutical sales professional looking to be part of an organization that values being curious, adaptable, and accountable? Lundbeck is a global biopharmaceutical company focusing exclusively on brain health. With more than 70 years of experience in neuroscience, we are committed to improving the lives of people with neurological and psychiatric diseases. Lundbeck employees are inspired and driven by our purpose to advance brain health and transform lives. Join us on our journey of growth!
We are seeking a dynamic and results-driven sales professional with a proven track record of success who is looking to grow with LundbeckOur ideal candidate will have the ability to be a specialty product expert with an understanding of requisite market complexities in order to be successful promoting our products to stakeholders in the primary care and neurology settings. As an Account Manager, you lead the promotion of our psychiatry portfolio, executing sales and marketing strategies with comprehensive clinical knowledge to drive sales performance. Our Account Managers are adept at executing against the toughest commercialization challenges in today's rapidly changing environment and must demonstrate strong capability in the following areas:
ESSENTIAL FUNCTIONS:
Business Planning & Account Leadership - Ability to use digital tools and apply data-based insights to create opportunities, develop strategy & tactics, allocate resources to enhance sales execution, monitor progress and adjust direction to maximize sales performance.
Selling - Deliver messages in a clear and compelling way to customers, effectively probe customer needs to handle objections, and close every call with a commitment to action to drive changes in behavior.
Customer Development - Build and maintain productive internal and external relationships based on customer needs and organizational goals, incorporating “total office” account management where applicable.
Local Market & Therapeutic Area Expertise - Gather and validate key trends and dynamics in the market, map account linkages, and apply comprehensive therapeutic knowledge to uncover and prioritize unique opportunities.
Reimbursement - Consistently demonstrate the ability to stay informed on reimbursement dynamics, anticipate and effectively address payer access issues (IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources.
Pharmaceutical Environment/Compliance - Apply knowledge of pharmaceutical and regulatory environment, including accountability and adherence to Lundbeck policies and procedures and FDA regulations regarding the promotion of pharmaceutical and medical products.
REQUIRED EDUCATION, EXPERIENCE and SKILLS:
Bachelor of Arts or Bachelor of Sciences degree from an accredited college or university
2-5 years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience.
Must demonstrate the intellectual capacity to score highly on disease and product training exams, including being certified on product knowledge annually
Self-starter, with a strong work ethic, tenacity, and outstanding communication skills
Adaptability: Ability to embrace change and work collaboratively in a fast-paced team environment.
Problem-Solving: Proven analytical skills to identify solutions and overcome obstacles.
Data Analysis: Strong computer and technical skills used in analyzing data to develop both short- and long-term goals aligned with business objectives.
Must live within 40 miles of territory boundaries
Driving is an essential duty of this job; must have a valid driver's license with a safe driving record that meets company requirements
Meeting and complying with reasonable industry-standard credentialing requirements of healthcare providers / customer facilities is required for continued employment with Lundbeck
Ability to lift, bend, push, pull and move items including, but not limited to equipment, pharmaceutical samples, and any other work-related materials up to 25 lbs. with or without reasonable accommodation.
PREFERRED EDUCATION, EXPERIENCE AND SKILLS:
Recent documented successful experience selling to general practitioners (GPs) and primary care centers.
Prior experience promoting and detailing products specific to CNS/neuroscience
Previous experience working with alliance partners (i.e., co-promotions)
TRAVEL:
Willingness/Ability to travel up to 30% - 40% domestically to (a) regularly meet/interact with customer base and internal personnel within assigned territory; and (b) typically attend 4-8 internal/external conferences and meetings spanning locations within the United States. Travel must be able to be completed in a timely manner.
The range displayed is a national range, and if selected for this role, may vary based on various factors such as the candidate's geographical location, qualifications, skills, competencies, and proficiency for the role. Salary Pay Range $108,000 to $125,000 and eligibility for a sales incentive target of $39,000. Benefits for this position include flexible paid time off (PTO), health benefits to include Medical, Dental and Vision, company match 401k and company car. Additional benefits information can be found on our career site. Applications accepted on an ongoing basis.
Why Lundbeck
Lundbeck offers a robust and comprehensive benefits package to help employees live well and protect their health, family, and everyday life. Information regarding our benefit offering can be found on the U.S. career site.
Lundbeck is committed to working with and providing reasonable accommodations to disabled veterans and other individuals with disabilities during our employment application process. If, because of a disability, you need a reasonable accommodation for any part of the application process, please visit the U.S. career site.
Lundbeck is proud to be an equal opportunity workplace. We are committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, and any other characteristic protected by law, rule, or regulation. Lundbeck participates in E-Verify.
Proposal Writer
Bonita Springs, FL job
The Proposal Writer/Analyst/Strategist will manage, develop, and lead a request for proposal project by working through the (a) development of strategic and client-focused proposal content, (b) written proposals, and (c) other sales-related documents for a variety of client audiences. The Proposal Writer/Analyst/Strategist is a key contributor on the Proposal team, accountable for analyzing assigned opportunities, creating competitively positioned content, and conveying a powerful corporate image to result in significant market share and profitability. This position strives to ensure timely and quality completion of assigned projects in accordance with company standards. This occurs, through a collaborative effort with the Proposal, Sales, Business Informatics, Underwriting, Pricing teams and cross-functionally with internal and external customers.
This position is required on-site 5 days a week.
Roles and Responsibilities
Ensure a proactive and strategic approach in support of client acquisition and retention efforts, including Requests for Proposals (RFPs), Requests for Information (RFIs), Best and Final Offers (BAFOs), client retention bids, and other support and sales-related documents.
Develop strategic activities, such as the creation of compelling content to position defined strategies for high-profile opportunities; process execution associated with timely completion; volume planning; and ongoing process enhancements.
Provide the Sales team with consultative support on the development and execution of targeted and opportunity-specific strategies to enhance the company's competitive advantage.
Utilize expert-level editorial, grammatical, and writing skills to ensure all written deliverables follow and demonstrate tactical, strategic, financial, and sales-capture decisions.
Ensure project coordination (e.g., planning, scheduling, organizing, and coordination), follow-up correspondence, and reporting.
Contribute to a collaborative environment where knowledge and experience is shared to build expertise and support other members to achieve aligned results.
Strive toward an expert-level understanding of internal processes and nuances of subject matter expert departments to unite these deliverables and create a cohesive and competitively positioned proposal.
Maintain a deep understanding and continuously develop knowledge of the company's sales strategies, target markets, and trends in those markets and how the company's products and services are/or may be utilized in the target markets.
Demonstrate flexibility and ability to work independently and in a team/collaborative environment.
Support and/or lead other duties as assigned.
Essential Background Requirements
Education: A minimum of a bachelor's degree or equivalent of years of experience.
Qualifications:
Minimum of five years related, professional experience, preferably in pharmacy benefit management, healthcare sales, and/or strategic proposal-related work.
Proven support of client acquisition and retention efforts, including Requests for Proposals (RFPs), Requests for Information (RFIs), Best and Final Offers (BAFOs), client retention bids, and other support and sales-related documents.
Effective verbal communication skills and advanced writing and editing expertise
Advanced expertise in strategic marketing message development, conceptual thinking, problem solving, and ability to interact with and present information to all levels of internal and external audiences.
Demonstrated project management proficiency, including managing and leading multiple tasks/projects in a high-pressure environment with competing priorities, within tight time frames.
Advanced experience with Microsoft Office products (e.g., Word, Excel, PowerPoint, Project). Customer Relationship Management software experience a plus.
Excellent math and organizational skills with a well-developed eye for detail.
The ability to consistently interact cooperatively and respectfully with other employees
Participate in, adhere to, and support compliance program objectives
Radiology Physician
Florida job
Specialty Needed: General Radiology BC/BE Requirements: BC Length Of Assignment: 1 Year Facility Type: Hospital Call Requirements: none My client in Florida has a need for a Breastl Radiologist for a long term assignment. Start date is January 10,2023 due to the credentialing time frame being between 60-120 days. Schedule is Monday through Friday 8a to 5p. There is no Call for this assignment. Procedures required are General Mammo, Breast - IR, Breast - MRI, Breast - US, Diagnistic - 2D, Screening 2D, Screening 3D. MQSA is required as well as Fellowship. Volume expectations are still TBD. Systems utilized are PACS System, Powerscribe, Clario Worklist.
Please respond with your most current/updated CV for immediate consideration.
Alliance Recruiting Resources, Inc.
Medical Assistant - Xray Technologist
Palm Beach, FL job
New Hires may receive UP TO $3,500 for BXMO and $5,000 for ARRT Sign-On Bonus!
Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring for patients with purpose and integrity. We care like family! Jump-start your career as a X-Ray Tech - Medical Assistant today with MD Now.
Benefits
MD Now, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:
Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation.
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
Free counseling services and resources for emotional, physical and financial wellbeing
401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service)
Employee Stock Purchase Plan with 10% off HCA Healthcare stock
Family support through fertility and family building benefits with Progyny and adoption assistance.
Referral services for child, elder and pet care, home and auto repair, event planning and more
Consumer discounts through Abenity and Consumer Discounts
Retirement readiness, rollover assistance services and preferred banking partnerships
Education assistance (tuition, student loan, certification support, dependent scholarships)
Colleague recognition program
Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence)
Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.
Learn more about Employee Benefits
Note: Eligibility for benefits may vary by location.
Come join our team as a Medical Assistant with BXMO license. We care for our community! Just last year, HCA Healthcare and our colleagues donated $13.8 million dollars to charitable organizations. Apply Today!
Job Summary and Qualifications
Seeking a X-ray Technician / Medical Assistant like you who provides expertise and to be a champion of patient care. We are an amazing team that works hard to support each other and are seeking a phenomenal addition like you who feels patient care is as meaningful as we do.
What you will do in this role:
Take vital signs, collecting lab specimens, performing EKG's, and administering IM injections.
Perform all x-ray/imaging services according to provider's orders and updates patient charts accordingly.
Collect patient history and documenting EHR appropriately.
You may apply splints, dressings and bandages.
Assist with check-in/check-out when needed including auditing charts.
Maintain records and logs on activities including in-house lab work, drug screens, and lab work sent out to other labs.
Keep patients and visitors informed of clinic progress.
You should have:
1+ year of clinical experience in a patient care setting is helpful.
Experience using an EHR system is beneficial.
High School Diploma or equivalent is required.
Graduate of an accredited school of Medical Assistants or completion of an approved program (BOTP) is required.
Radiological Technologist (RT) or Basic X-ray Machine Operator (BMXO / BMO), license is required in state of residency.
Current certification from the American Association of Medical Assistants (AAMA) is preferred.
Current BLS Certification is required within 30 days of start.
Must obtain a Federal Breath Alcohol Screening Certification and Federal Drug Screening Certification within 3 months of employment or promotion.
MD Now is the largest provider of urgent care services in Florida with 60+ conveniently located clinics across Indian River, Palm Beach, Broward, Miami-Dade, Lee, Manatee, Sarasota, Seminole, and Hillsborough counties. Our state-of-the-art, physician-led clinics are open 365 days a year, giving patients easy access to healthcare they can trust. Patients are typically treated in under an hour, without an appointment, making MD Now the ideal healthcare solution for patients of all ages. We treat many injuries and illnesses. We provide lab testing, digital X-rays, EKGs, Occupational Health, vaccinations and immunizations. We can also provide physicals for school, camp, sports or work. Our facilities provide COVID-19 evaluations, testing and vaccines as well. MD Now is an affiliate of HCA Healthcare.
HCA Healthcare has been recognized as one of the World's Most Ethical Companies by the Ethisphere Institute more than ten times. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses.
Director of Pharmacy Operations
Lakeland, FL job
YOUR PASSION, ACTIONS & FOCUS is our Strength
Become one of our Contributors
Join the KnipperHEALTH Team!
Under the direction of the Vice President of Pharmacy Operations, the Director of Pharmacy Operations provides site leadership and operational oversight to ensure the safe, compliant, and efficient dispensing of prescription products nationwide. This role is accountable for achieving strategic, financial, and operational goals across a multistate, high-volume pharmacy enterprise. The Director of Pharmacy Operations will oversee a highly automated fulfillment environment and drive continuous improvement initiatives to ensure optimal scalability, quality, and patient satisfaction.
This role is located ON-SITE at our facility in Lakeland, Florida. Occasional overnight travel as needed for training, collaboration, and leadership meetings may be required (
Develops and maintains pharmacy services in accordance with State and Federal regulations, accepted standards, professional practices, and company policies in coordination with the Pharmacists-in-Charge.
Leads operations supporting multi-state licensor, ensuring readiness for shipment to all 50 states, including oversight of pharmacist and pharmacy licensing, state-specific compliance requirements, and audit readiness.
Oversees high-volume automation and robotic dispensing systems and associated vendor relationships, including configuration, maintenance, and performance optimization, ensuring seamless integration with the pharmacy management system.
Ensures maintenance and optimization of robotic systems, conveyor networks, and automated labeling, counting, and packaging systems to support national-scale prescription volume.
Provides strategic oversight of cold-chain management processes for temperature-sensitive medications, including monitoring, packaging validation, facilities, equipment, and excursion management programs and systems to ensure product integrity.
Oversees management of inventory control and pharmacy supplies, including forecasting, purchasing, storage, reconciliation, and waste reduction to support continuous operations and minimize stock-outs.
Oversees the planning, supervision, coordination, and execution of all activities related to pharmacy operations, including prescription processing, fulfillment, packaging, and logistics.
Provides on-site operational support to the data entry and clinical review teams, ensuring efficient communication, issue escalation, and work-flow alignment-while maintaining collaborative partnership with the remote Director having direct supervision responsibility for those functions.
Monitors operational throughput, production metrics, and key performance indicators (KPIs) to drive efficiency, reduce error rates, and maximize resource utilization.
Coordinates and supervises departmental operations, including but not limited to hiring, determining workload, delegating assignments, training, monitoring, scheduling, evaluating performance, and initiating corrective and disciplinary actions.
Mentors, trains, and develops staff and management team to support career growth and succession planning.
Collaborates cross-functionally with Compliance, Quality, IT, Human Resources, and Talent Acquisition
Oversees quality improvement initiatives and ensures standard operating procedures (SOPs) reflect best practices in automation, fulfillment, safety, and patient care.
Partners with IT and vendor partners to validate system upgrades and implement process automations to enhance operational capacity.
Supports the annual budgeting process, including forecasting for technology upgrades, cold-chain infrastructure, automation expansion, inventory management systems, and compliance costs.
Maintains strict adherence to HIPAA and other confidentiality requirements, protecting patient data and proprietary business information
Serves as the primary on-site point of contact for client and manufacturer relationships, facilitating effective communication, resolving operational issues, and ensuring contractual and service-level agreements (SLAs) are met.
Enforces company policies and procedures and performs other duties as assigned.
The above duties are meant to be representative of the position and not all-inclusive.
MINIMUM JOB REQUIREMENTS:
5+ years of progressive pharmacy operations leadership, preferably within a central fill, mail-order, or specialty pharmacy environment.
Advanced degree (PharmD and MBA, or equivalent) preferred.
Demonstrated experience managing large-scale automated pharmacy systems (e.g., robotic dispensing, high-speed packaging, or conveyor networks).
Experience with Pharmacy Management System software platforms
Proven experience with multi-state licensure, nationwide distribution, and familiarity with state board regulations across multiple jurisdictions a requirement
Experience overseeing cold-chain operations and managing temperature-sensitive pharmaceutical products.
Experience managing large-scale inventory and supplies operations within a regulated pharmacy or healthcare environment.
Pharmacist licensure in one or more key states - including AL, CO, FL, ID, IL, IN, KY, LA, MD, MI, MS, OR, TN, TX, VA, and WV - is highly desirable but not required.
KNOWLEDGE, SKILLS & ABILITIES:
Excellent leadership and management skills
Ability to effectively package data/metrics and present information to senior leadership
Proficient in MS Word, Excel, Power-Point, Outlook, and Visio.
Excellent written and verbal communication skills
Excellent analytical, problem solving and decision-making skills
Ability to accept changing workflows and unexpected demands requiring flexibility
Ability to work under pressure and appropriately prioritize responsibilities
Ability to work independently with minimal supervision
Ability to develop collaborative working relationships
PHYSICAL DEMANDS:
Location of job activities 100% inside
Noise and/or vibrations exposure
Reaching (overhead), handling, and feeling
Stand and sit for prolonged periods of time
Lift, carry, and move up to 50 pounds
This position is in a typical office environment which requires prolonged sitting in front of a computer. Requires hand-eye coordination and manual dexterity sufficient to operate standard office equipment including operation of standard computer and phone equipment. May have occasional high stress when dealing with customers/clients.
Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
#Director#PharmacyOperations#Lakeland
Knipper Health is an equal opportunity employer
Compounding Inventory Coordinator - 503A Pharmacy
Miami Gardens, FL job
About Us
At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience.
Core Values
The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability.
Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs
Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes
Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients.
You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services.
Job Summary:
We are looking for a dependable and detail-focused Compounding Inventory Coordinator to oversee and maintain stock levels of all Active Pharmaceutical Ingredients (APIs), excipients, and supplies within our 503A compounding pharmacy. This role ensures the compounding team has timely access to all materials needed to produce customized medications safely and efficiently, in full compliance with USP 795, 800 and state board regulations.
Key Responsibilities:
Inventory Oversight
- Maintain real-time inventory of APIs, excipients, bases, and packaging components
- Ensure proper labeling, storage, and tracking of all materials in accordance with USP and 503A regulations.
- Stage ingredients for daily formulations and batch preparations ahead of schedule.
- Conduct daily/weekly cycle counts and reconcile discrepancies proactively
Regulatory Compliance & Documentation
- Record all incoming shipments, including lot numbers, expiration dates, and Certificate of Analysis (COA) documentation.
- Monitor for near-expiry or quarantined products and communicate with supervisor immediately
- Maintain clean, organized, and segregated storage areas for hazardous and non-hazardous items
- Ensure compliance with USP 800 hazardous drug handling and storage standards (where applicable)
Operational Support
- Coordinate with pharmacists and compounders to anticipate material needs for upcoming formulas
- Communicate shortages or overstock issues to procurement and management
- Support internal audits, DEA inspections, and regulatory reviews with accurate documentation
Receiving & Labeling
- Receive materials and verify them against purchase orders
- Apply internal barcoding or tracking labels upon receipt
- Store materials under proper environmental conditions (e.g., refrigeration, flammables cabinet etc.)
Qualifications:
- High school diploma or GED (required); Associates degree or pharmacy technician certification
- preferred
- 1-2 years of experience in a compounding pharmacy or healthcare inventory environment
- Familiarity with USP 795, 797, 800 and 503A compounding practices (preferred)
Skills & Competencies
- Strong organizational and multitasking skills
- Attention to detail and ability to maintain compliance-focused records - Ability to lift up to 50 lbs. and work on your feet for extended periods
- Proficiency with inventory systems and Microsoft Excel
- - Clear written and verbal communication
Job Type: Full-time - 100% On Site
Expected Hours: 40 hours per week
Work Schedule:
Monday - Friday, 9 AM - 5:30 PM
Pay Range$44,000-$55,000 USD
Benefits:
401(k) with up to 4% matching
Medical, dental, vision and life insurance
Paid time off
Paid public holidays
At The Pharmacy Hub, we don't just offer jobs-we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success.
If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.
Auto-ApplyMDS Coordinator (LPN or RN)
Lake Worth, FL job
Are you a dedicated nursing professional with a passion for ensuring top-tier patient care? Avante at Lake Worth Skilled Nursing and Rehabilitation Center is seeking an MDS Coordinator to oversee and coordinate resident assessments, ensuring compliance with federal, state, and local regulations. If you're looking for a role that truly makes an impact, we invite you to join our compassionate and driven team!
Why Avante?
At Avante, we believe in providing the highest quality of care to our residents while fostering a supportive and rewarding work environment for our team.
Benefits You'll Love:
? Competitive Compensation
? Comprehensive Insurance Coverage (Medical, Dental, Vision and more!)
? Strong Retirement Plan for Your Future
? Paid Time Off & Holidays to Recharge
? Tuition Reimbursement - Invest in Your Education
? Health & Wellness Programs to Keep You Feeling Your Best
? Employee Recognition Programs - Win prizes & an annual cruise!
? A Collaborative Work Environment - We value your voice! (Employee surveys, check-ins, & town halls)
? Advancement Opportunities - Grow Your Career with Us!
Avante Offers DAILY PAY!! Work Today, Get Paid Today!
Key Responsibilities:
Conduct and coordinate the Minimum Data Set (MDS) assessments and care planning in compliance with all regulations.
Ensure timely and accurate submission of MDS assessments to the State Repository per RAI Manual guidelines.
Work closely with the Interdisciplinary Care Team to determine appropriate assessment review dates.
Evaluate and update resident care plans to reflect any changes in health status or quarterly assessments.
Monitor and analyze Quality Measures Reports, with an emphasis on maintaining high Five-Star Ratings.
Educate and collaborate with nursing staff, residents, and families to develop personalized care plans.
Participate in facility surveys and inspections conducted by regulatory agencies.
Maintain strict confidentiality and uphold Avante's commitment to compliance and patient privacy.
What We're Looking For:
? Active, unencumbered Licensed Nurse (LPN/RN) in the state.
? Nursing Degree/Diploma from an accredited school, college, or university.
? 2+ years of experience in a hospital, skilled nursing, or healthcare facility preferred.
? Strong knowledge of nursing practices, medical procedures, and regulatory guidelines.
? Leadership skills with the ability to motivate and collaborate with interdisciplinary teams.
? Excellent organizational and critical thinking abilities.
? Compassion, patience, and a positive attitude toward residents and team members.
If you are passionate about patient care and rewarding work environment, Don't Hesitate- Apply Today!
Avante provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, Veterans' status, national origin, gender identity or expression, age, sexual orientation, disability, gender, genetic information or any other category protected by law. In addition to federal requirements, Avante complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Avante expressly prohibits any form of workplace harassment based on race, color, religion, sex, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, Veterans' status or any other category protected by law. Improper interference with the ability of Avante's employees to perform their job duties may result in discipline, up to and including, discharge.
Pharmaceutical Sales Representative, Endocrinology (Rare Disease) - Miami
Florida job
Achieve territory sales goals by promoting products and services to physicians and other medical personnel within assigned geography. Educate customers on the appropriate use, characteristics, and approved indications of products. Professionally represent the company and ensure high levels of visibility and customer service in territory. Maintain effective communication and relationships with key external and internal customers.
Responsibilities
Effectively promote and educate specialty physicians on the appropriate use of rare disease products through one-on-one meetings and group presentations, company-approved promotional speaker programs and other company-approved means.
Responsible for achieving both territory product sales goals and territory sales activity goals through company defined metrics.
Ensure high performance levels of call and field productivity. Meet territory product sales goals while adhering to all defined ethical sales practices, compliance guidelines and required promotional regulations
Execute company-approved Product Marketing plans and territory/regional business plan activities
Support targeted customers and accounts using company-approved resources, sales materials and promotional activities/programs/initiatives as identified by Sales Leadership
Appropriately managing/maintaining all company equipment and company-approved promotional materials (e.g., sales materials, company literature, product samples, etc.) according to defined company compliance guidelines
Ensure optimum territory sales strategy execution using territory business plans, regional business plans and all appropriate sales reports
Communicate cross-functionally to gather knowledge of best practices from peers within the organization.
Attend all company-sponsored sales and medical related meetings as directed by company management.
Actively pursue continuous learning and professional sales development on effective sales/communication techniques and product/therapeutic area knowledge.
Qualifications
BA/BS required
5-7+ years of successful pharmaceutical sales experience required. Previous experience in competitive markets preferred
Proven record of sustained high sales performance and achievement (Top 10%, National Awards)
2+ years of experience promoting rare competitive disease products strongly preferred
A valid, US State-issued driver's license is required
Launch experience or start-up experience is a plus
Experience working with Endocrinologists preferred
Deep understanding of all stakeholders in an office and ability to support them in getting a patient started on therapy within guardrails established by the company
Demonstrated ability to both build relationships within existing accounts as well as proactively find new accounts
Previous experience working with specialty pharmacies and internal patient support roles preferred
Experience navigating managed care and rare disease products preferred
At Xeris, performance consists of both results and behaviors. Behavioral competencies include: Leadership skills, Teamwork & Collaboration, Attention to Detail, Self-Starter, Problem Solving, Organizational skills, Adaptability, Professionalism, Written and Verbal Communications, Adherence to compliance policies and processes, Analytical skills, Multi-Tasking skills, Decision-making skills, Accountability, Inquisitive
Working Conditions: Position may require periodic evening and weekend work, as necessary to fulfill obligations. Periodic overnight travel. Position requires vehicle travel, as necessary. Travel approximately 70%.
The level of the position will be determined based on the selected candidate's qualifications and experience.
#LI-REMOTE
As an equal employment opportunity and affirmative action employer, Xeris Pharmaceuticals, Inc. does not discriminate on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. It is our intention that all qualified applications are given equal opportunity and that selection decisions be based on job-related factors.
The anticipated base salary range for this position is $110,000 to $190,000. Final determination of base salary offered will depend on several factors relevant to the position, including but not limited to candidate skills, experience, education, market location, and business need. This role will include eligibility for commission and equity. The total compensation package will also include additional elements such as multiple paid time off benefits, various health insurance options, retirement benefits and more. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.
Auto-ApplyAssociate Director - Medical Science Liaison- Dermatology - North Florida
Tampa, FL job
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Associate Director- Medical Science Liaison Dermatology - North Florida - Position requires home-base location in the Orlando, FL or Tampa Bay, FL
1.0 Purpose:
Scientific and Clinical Experts (SEs/CEs) are individuals who are noted for their expertise in a therapeutic area and as a result have special needs for in-depth and cutting-edge information, because they treat patients, design and implement novel research, and educate colleagues and students. The Medical Science Liaison (MSL) program is specifically designed to meet these needs through a field-based group of medical professionals with deep content knowledge about specific disease states, Lilly and competitive compounds and the landscape within the therapeutic areas they represent. MSLs recognize and communicate feedback and insights of strategic importance from their interactions with SEs and CEs, to better inform Lilly's strategic direction for research and commercialization. By facilitating scientific exchange between industry and the scientific community, MSLs have the opportunity to shape the future of healthcare by providing needed information that addresses important clinical and scientific questions.
2.0 Responsibilities:
Scientific knowledge
MSLs will be required to engage in continuous learning to maintain the highest level of technical expertise within the therapeutic area they represent. This will enable the MSLs engagement in scientific exchange to respond to the diverse medical information needs based on customer requests. As a result, the MSL will establish themself as a reliable, trusted, resource of unbiased, accurate, up-to-date, medical and scientific information requested by their customers.
Customer engagement
MSLs will spend the majority of their time on customer facing activities. Through the application of emotional intelligence, strategic thinking and a deep understanding of their customers, MSLs will act as one of the primary interfaces between Lilly medical and SEs/CEs to deliver a positive customer experience and utilize MSL capabilities that enhance customer engagement. Additionally, MSLs connect SEs/CEs with other Lilly resources or internal business partners as appropriate and facilitate collaborative research and external opportunities.
Territory ownership
MSLs will be expected to demonstrate strategic analysis, planning, and prioritization to maximize efficiency. They will implement and evaluate a strategic territory plan prioritizing core MSL activities and take personal accountability for results. There is also an expectation for compliant partnerships across all Lilly field roles sharing customers to create an appropriately coordinated experience. MSL will effectively utilize territory analytics for customer identification and routing prioritization.
Strategic vision and leadership
MSLs effectively synthesize and communicate actionable customer/clinical insights to internal Lilly medical and cross functional teams. MSLs use good judgement in decision-making and escalate issues as appropriate. They cultivate internal networks and collaborate effectively across functions including working closely with other field-based colleagues. They embrace change, exercise strategic agility with evolving business needs and utilize innovative resources.
MSLs should demonstrate the Team Lilly Behaviors (Include, Innovate, Accelerate, and Deliver) at all times in their work with peers and other Lilly colleagues. Within their own team, MSLs are expected to contribute to team goals and be an effective teammate. The MSL will execute the role in a compliant manner, adhering to all governing internal and external requirements, procedures, and laws, demonstrating good judgement at all times.
3.0 Minimum Requirements:
Advanced degree in health sciences (e.g., PharmD, MD, PhD in a medically related field) required with 2-3 years of relevant clinical or therapeutic area experience desired. OR-
Masters or bachelor's level degree in health sciences (e.g. BSN, RPh, PA, NP) considered if 5 or more years clinical, research or industry experience in relevant therapeutic area is present.
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and/or visas for this role.
Valid U.S. driver's license and acceptable driving record.
4.0 Other Information/Additional Preferences:
• Field based position requires ability to travel up to 80% and work up to 4 to 6 weekends a year.
• Applicants should live in close proximity to a transport hub (airport/train station).
• Intellectual curiosity about the field of science/medicine for which they are responsible.
• Learning agility to comprehend and effectively communicate large amounts of complex scientific content in a clear and concise fashion.
• Self-directed and able to work alone in the field effectively managing multiple priorities and projects.
• Advanced presentation and computer skills with expertise in literature identification.
• Effective strategic and critical thinking in order to analyze, assess and evaluate information and interpret impact or relevance to future states.
• Excellent verbal and written communication skills.
• Ability to use field-based electronic or other communication tools for all aspects of job is critical.
• Resiliency in managing complex challenges.
• Strong teamwork and interpersonal skills, including high emotional intelligence and the ability to engage in professional relationship building and networking.
• Experience in servicing customer needs for complex information.
• Significant experience in professional networking with mutually beneficial outcomes.
• Experience in field based working environment highly valued.
• Familiarity with health systems, academic communities, medical research, and medical education process highly valued.
• Dermatology therapeutic area experience is strongly preferred.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$151,500 - $244,200
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Auto-ApplyArea Business Specialist, Neurology (Rare Disease) - Florida
Florida job
Achieve territory sales goals by promoting products and services to physicians and other medical personnel within assigned geography. Educate customers on the appropriate use, characteristics and approved indications of products. Professionally represent the company and ensure high levels of visibility and customer service in territory. Maintain effective communication and relationships with key external and internal customers.
Responsibilities
* Effectively promote and educate Specialty physicians on the appropriate use of rare disease products through one-on-one meetings and group presentations, company-approved promotional speaker programs and other company-approved means.
* Ensure high performance levels of call and field productivity. Meet territory product sales goals while adhering to all defined ethical sales practices, compliance guidelines and required promotional regulations
* Execute company-approved Product Marketing plans and territory/regional business plan activities
* Support targeted customers and accounts using company-approved resources, sales materials and promotional activities/programs/initiatives as identified by Sales Leadership
* Appropriately managing/maintaining all company equipment and company-approved promotional materials (e.g., sales materials, company literature, product samples, etc.) according to defined company compliance guidelines
* Ensure optimum territory sales strategy execution using territory business plans, regional business plans and all appropriate sales reports
* Attend all company-sponsored sales and medical related meetings as directed by company management.
* Responsible for achieving both territory product sales goals and territory sales activity goals through company defined metrics
* Actively pursue continuous learning and professional sales development on effective sales/communication techniques and product/therapeutic area knowledge.
Qualifications
* BA/BS required - 2+ years of experience promoting rare disease products
* 5-7+ years of successful pharmaceutical sales experience
* A valid, US State-issued driver's license is required
* Strong knowledge of sales processes and rare disease products
* Proven record of sustained high sales performance and achievement
* Competencies: Leadership skills, Teamwork & Collaboration, Attention to Detail, Self-Starter, Problem Solving, Organizational skills, Adaptability, Professionalism, Written and Verbal Communications, Analytical skills, Multi-Tasking skills, Decision-making skills, Accountability
* Internal candidates who have been promoted from a retail Inside Sales Representative position to a Rare Inside Sales Representative position may be eligible to apply for this role, as are current Territory Business Managers. Internal applicants may qualify based on demonstrated performance, product expertise, and readiness for field responsibilities, even if the requirements posted in the for external candidates are not met.
* Working Conditions
* Position may require periodic evening and weekend work, as necessary to fulfill obligations. Periodic overnight travel.
* Travel up to 70%
The level of the position will be determined based on the selected candidate's qualifications and experience.
#LI-REMOTE
As an equal employment opportunity and affirmative action employer, Xeris Pharmaceuticals, Inc. does not discriminate on the basis of race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. It is our intention that all qualified applications are given equal opportunity and that selection decisions be based on job-related factors.
The anticipated base salary range for this position is $110,000 to $190,000. Final determination of base salary offered will depend on several factors relevant to the position, including but not limited to candidate skills, experience, education, market location, and business need. This role will include eligibility for commission and equity. The total compensation package will also include additional elements such as multiple paid time off benefits, various health insurance options, retirement benefits and more. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.
Auto-ApplyMachinist III
Noven Pharmaceuticals job in Miami, FL
Overview A Machinist operates and maintains several fabrication equipment like lathes and milling machines. They review drawings or samples to ensure accurate production; take precise measurements for cutting/shaping tasks using appropriate machine settings.
Provides technical support to manufacturing, engineering and other departments. Works on assignments that may be complex in nature and where considerable judgment and initiative may be required to resolve electrical, electromechanical or mechanical problems and make recommendations. Applies standard electrical, mechanical, electromechanical, and /or optical procedures and tests in such areas as manufacturing, development, maintenance, quality, testing, and engineering. Constructs, inspects, adjusts, tests, documents and maintains equipment, components, devices and systems following proper procedures and instructions. Provides guidance, training and direction to less seasoned employees. Creates/edits maintenance procedures.
Responsibilities
Operate machine tools such as lathes, milling machines, and grinders to produce metal parts.
Review electronic or written blueprints or specifications for a job.
Plan the sequence of cutting and finishing operations.
Check accuracy of work against blueprints and specifications.
Machine parts to specifications, using machine tools, such as lathes, milling machines, shapers, or grinders.
Measure, examine, or test completed units to check for defects and ensure conformance to specifications, using precision instruments, such as micrometers.
Measure dimensions of completed products or workpieces to verify conformance to specifications.
Maintain machine tools in proper operational condition.
Study sample parts, blueprints, drawings, or engineering information to determine methods or sequences of operations needed to fabricate products.
Design fixtures, tooling, or experimental parts to meet special engineering needs.
Design tools, fixtures, or other devices for production equipment.
Communicate with engineering, supervisory, or manufacturing personnel to exchange technical information.
Evaluate machining procedures and recommend changes or modifications for improved efficiency or adaptability.
Dismantle machines or equipment, using hand tools or power tools to examine parts for defects and replace defective parts where needed.
Disassemble equipment for maintenance or repair.
Replace worn equipment components.
Install repaired parts into equipment or install new equipment.
Follows Standard Operating Procedures, Protocols, Work Orders, Company Policies, and work instructions from supervisors in the course of performing his / her work functions. Performs all work in adherence to the Company's cGMP and safety standards and procedures.
Maintains, organizes, and keeps all engineering and other company documentation associated with Noven's manufacturing equipment in an orderly manner. Leads the development and improvement of these documents, such as maintenance and equipment operational instructions, and implement changes following applicable quality system and compliance requirements.
Sets up, adjusts, operates, maintains and cleans any of Noven's manufacturing equipment. Selects appropriate tools and instrumentation to carry out these functions, and ensures that these are properly calibrated and are fully functional before being used. Provides new techniques to improve existing maintenance systems.
Accurately inspects and measures critical aspects of electromechanical components; creates and/or follows engineering drawings, and wiring diagrams. Works from specifications, drawings, manuals, sketches and verbal instructions.
Able to accurately measure and inspect mechanical, electromechanical or electrical parts and equipment using complex metrology equipment (oscilloscope, voltmeters, indicators, comparators, microscopes, micrometers, etc).
Prepares tool carts on time, according to production schedules.
Maintains a clean and orderly work environment. Practices safe work habits and completes required safety and environmental hazard training. Able to interpret MSDS sheets.
Examines equipment, machinery, building components and associated mechanical and electrical components to determine condition and need for work and determines need for replacement parts or repairs. Able to search for hard to find items using a search engine in a computer.
Assist with the fabrication of new or custom-built manufacturing, research, development, and test equipment. Including software and hardware related development.
Applies an extensive practical experience and knowledge base to develop alternative solutions to electrical / electronic or mechanical problems which may be of a difficult and / or unusual nature.
Accurately complete the required documentation (logbooks, work orders, data entry, data sheets etc.) pertaining to installation, maintenance, spare parts holding and trouble-shooting of Noven's manufacturing equipment.
Work closely with team and group members to achieve defined goals, and communicate effectively in recording work performed, and in offering feedback and improvement recommendations based on observations and work experience.
Performs operational functional testing, troubleshooting and debugging of components, sub-assemblies and systems to isolate faults and suggest remedies and recommendations for changes in product or test method in a team environment
Writes technical reports and develops charts, graphs and schematics to describe and illustrate systems/tests operating characteristics, malfunctions, deviations from design specifications, and functional limitations.
Executes IQ/OQ protocols related to equipment installation and/or modification. Performs process/product tests and audits for conformity to quality and/or regulatory requirements. Records test procedures and results.
Performs such individual assignments and related duties as the supervisor may direct; establishes and maintains effective work relationship within the department, facility and company.
Works with Manufacturing, QC and R&D to quickly resolve unscheduled technical issues to minimize downtime on the production line or business impact.
Exhibits a positive and customer focused attitude that promotes team work across the organization.
Orders materials needed for repairs, manages vendor selection for outside work based on quality and cost of services following company financial policies.
Effectively manages multiple vendors to ensure on-time delivery of instruments, proper documentation of results is provided and on-site services are performed adequately per company guidelines.
Collaborate with Engineering and/or other technical team members to determine root cause and corrective and preventative actions during investigation events associated to equipment technical issues.
Ability to multitask and assess priorities to meet company timelines.
Maintains a clean and orderly work environment and contributes to the company's 6S program.
Maintains compliance to training requirements.
Communicates effectively with personnel at all levels and effectively participates in a team environment.
Ability to escalate unresolved issues per company guidelines to ensure resources are allocated and issues are communicated across cross-functional teams. Inform appropriate personnel of problems or concerns in a timely manner.
Contributes to the department's overall financial goals through the identification and implementation of cost reduction ideas.
Manages purchase requisitions, purchase orders, invoices and quotes associated to Calibration and provides support to finance on these documents.
Ability to train peers on maintenance and troubleshooting best practices and techniques.
Initiates and assists in completion of Notice of Events investigations due to technical equipment malfunction, including preliminary impact assessment, probable root cause and preliminary corrective action.
Support Engineering projects and product development activities without impacting critical path.
Qualifications
Education / Experience:
High school diploma or GED required
8+ years working with machine tools or mechanical assembly
High level of blueprint, technical drawings, schematics reading required
Strong verbal communication and problem-solving skills
Attention to detail and ability to deal with complexity
Capable of working in a company-focused, deadline-driven environment while maintaining a positive attitude
Experience using measuring tools and gages
Vocational school or apprenticeship preferred
Excellent manual dexterity, accuracy and attention to detail
Great verbal and written communication skills
Experience in using and/or semi-automated tools and machines (lathes, grinders etc.)
Judgement / Decision Making:
Works on assignments that may be complex in nature where considerable judgment and initiative are required in resolving problems and making recommendations. May determine methods and procedures on new assignments and may provide guidance to other non-exempt personnel.
Sign off work order utilizing company enterprise system
Advise supervisor of technical advancements to increase production
Develop and maintain effective working relationships with peers, supervisors, and other staff
Monitor and document operational and performance issues and provide feedback to supervisor
Work Environment:
While performing the duties of this Job, the employee is regularly exposed to moving mechanical parts. The noise level in the work environment is usually moderate. May be required to work in areas where high noise hazards prevail. May be exposed to fumes or airborne particles. Majority of work performed with exposure to chemicals, electrical current, fumes, moving parts, noise, and odors.
Physical Demands:
Frequently required to walk; use finger and hands, handle, or feel; reach with hands and arms and talk or hear.
Occasionally required to sit; climb or balance and stoop, kneel, crouch, or crawl.
Occasionally required to lift and carry objects weighing up to one hundred (100) pounds.
Standing is often required, as well as stooping and bending. Visual acuity and manual dexterity required when performing essential duties; carelessness could result in injury.
Specific vision abilities required by this job include close vision, distance vision, peripheral vision and ability to adjust focus.
Auto-ApplyInventory Supervisor
Miami Gardens, FL job
About Us
At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience.
Core Values
The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability.
Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs
Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes
Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients.
You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services.
The Pharmacy Hub is looking for Inventory Supervisor to join our Logistic Department at our Miami Gardens and Davie Pharmacy locations. If you have a strong background in inventory control, team management, and process improvement, this is your chance to take a leadership role in ensuring our inventory is accurate, efficient, and aligned with business goals.
Key Responsibilities
Supervise, organize, and control inventory levels to maintain steady product flow without overstocking or shortages
Implement inventory control procedures and lead continuous improvement initiatives
Coordinate with purchasing, warehouse, production, and sales departments for seamless product supply
Oversee physical audits, cycle counts, and inventory reconciliations to ensure accuracy
Generate reports on inventory turnover, losses, obsolescence, and operational efficiency
Manage, train, and evaluate a team of inventory assistants or analysts
Utilize ERP and WMS systems for automated inventory management
Establish and enforce policies for handling defective, obsolete, or excess products
Identify and implement layout and process improvements within the inventory area
Participate in additional projects as assigned by the Inventory Manager
Qualifications
Minimum 2-3 years experience in an inventory role with supervisory responsibilities
Strong numerical aptitude and analytical skills for data-driven decision making
Proficiency in Microsoft Excel and inventory management software (ERP/WMS)
Excellent multitasking, communication, and interpersonal skills
Ability to work in a fast-paced environment, manage receiving operations, and maintain accurate stock levels
Self-starter with strong problem-solving abilities
Flexible availability including weekends and night shifts
Bilingual (English/Spanish) is a plus
Work Environment & Physical Demands
Fast-paced pharmacy and warehouse setting at the Davie Pharmacy
Exposure to loud noises and non-climate-controlled areas
Frequent standing, bending, lifting, carrying, pushing, pulling, and stacking (up to 50 lbs)
Regular use of computer terminals and mobile devices
Work Schedule & Compensation
Full-time, 44 hours per week (9:00 AM - 6:00 PM)
Hourly Rate: $23.00
Benefits:
401(k) with up to 4% matching
Medical, dental, vision and life insurance
Paid time off
Paid public holidays
At The Pharmacy Hub, we don't just offer jobs-we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success.
If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.
Auto-ApplyTechnician II
Noven Pharmaceuticals job in Miami, FL
Provide technical support to manufacturing, engineering and other departments / teams by ensuring maximum equipment uptime, and addressing technical challenges. When not supporting manufacturing, technician shall perform scheduled PMs in timely manner as required by the CMMS system for work orders. Lastly, under limited supervision, performs and documents moderately complex technical functions relating to test, layout, quality control, fabrication, modification and assembly of mechanical equipment and/or components.
Responsibilities
Ensures maximum uptime of manufacturing equipment by completing preventive maintenance requirements.
Provide continuous feedback on preventive maintenance effectivity and improvements to the instructions based on usage and experience.
Executes scheduled Preventive Maintenance on manufacturing equipment in timely manner to always meet due dates.
Works with manufacturing to monitor and quickly resolve technical issues on manufacturing equipment.
Perform or assist with any production operation to maintain work flow or prevent downtime per production requests.
With minimal supervision, performs moderately complex testing, troubleshooting, debugging, installation and repair of components, sub-assemblies and systems to isolate root cause and suggest remedies.
Performs in-house inspection, maintenance and cleaning of all tooling required for changeovers within all areas of production.
Prepares and provides manufacturing with tooling required for changeovers per production schedule.
Execute repeatable setup procedures, maintains and cleans semi-complex manufacturing equipment and performs equipment alignment for each size/product. Must know all setup requirements for manufacturing lots.
Must be able to identify issues encountered during day to day tasks, diagnose its cause and develop and implement a solution.
Ensures equipment/tooling is properly calibrated / inspected before using.
With training provided, demonstrates the ability to operate machinery to produce components and products.
Reads and follows SOPs, work instructions and protocols. Contributes to the development and improvement of these documents.
Accurately documents changes to any equipment used in the development, testing or manufacture of products as per respective SOPs, i.e. in logbooks, work orders, data entry, data sheets, etc.
Verify GMPs and safety standards are maintained at all times and take action and/or follow-up when deficiencies are noted.
Follow lockout/tag out procedures.
Maintains a clean, orderly and organized work environment. Practices safe work habits and completes required safety and environmental hazard training. Able to interpret MSDS sheets.
May work closely with engineers or other technical team members during process development using limited documentation and only general support. May offer feedback and improvement recommendations based upon findings.
With necessary guidance, records test procedures and results, numerical and graphical data, and recommendations for changes in product or test method.
Performs updates to the SOPs related to role, as well as to PM instructions.
Able to use metrology equipment (indicators, comparators, microscopes, micrometers, etc.).
Ability to multitask and assess priorities.
Able to read and understand engineering drawings. AutoCAD or SolidWorks skills are desired.
Communicates effectively with personnel at all levels and effectively participate in a team environment, particularly for effective shift transitions.
Inform appropriate personnel of improvement ideas, problems or concerns.
Must be able to work additional hours, or beyond standard schedule, including holidays and weekends with little or no notice.
Maintains Noven's compliance training.
Qualifications
Competencies:
Must have intermediate knowledge of mechanical, hydraulic, pneumatic and electrical systems.
Strong writing and oral skill as well as technical editing skills.
Ability to work independently with minimal supervision within established procedures, providing efficient, effective and reliable services.
Ability to work with internal and external constituents
Able to make appropriate decisions with minimal intervention
Knowledge of proper power tools usage.
Ability to contribute to a team environment.
Excellent organizational skills.
Strong communication skills
Computer literacy in Microsoft Office is preferred.
Education / Experience:
Associate's Degree (AA or AS) or equivalent; or trade/technical schooling and 5-9 years of related experience and/or training; or the equivalent combination of education and experience. Pharmaceutical industry work experience is a plus. Ability to use computer and associated software.
Judgment / Decision Making:
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Use detail-oriented problem solving skills to assist in solving difficult mechanical or electrical issues. Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form
Work Environment:
Production/plant floor - pharmaceutical products
Physical Demands:
The employee will be occasionally required to climb or balance; stoop, kneel, crouch, or crawl; and smell. The employee must be able to lift and/or move up to 100 pounds.
Auto-ApplyMulti-Specialty Portfolio Specialist/Associate Portfolio Specialist (Sarasota, FL)
Sarasota, FL job
Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early- to late-stage investigational assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website ********************************** or follow us on LinkedIn.
Job Overview
We are currently seeking a dynamic, highly motivated individual for the position of Multi-Specialty Portfolio Specialist/Associate Portfolio Specialist.
This position is being posted at multiple levels.
Applicants for this position will be considered for the titles listed in this posting. The title and salary will be determined by the experience and qualifications of the final candidate.
Candidates who do not meet all of the qualifications may be considered for an Associate level role.
In this field-based role, the Multi-Specialty Portfolio Specialist/Associate Portfolio Specialist will focus on achieving sales goals within primary care, urology, and the women's health therapeutic area in an assigned geographic territory. This individual will have a proven record of success within specialty biopharmaceuticals. They will be highly collaborative, tactical, energetic and thrive in a nimble organization.
The Multi-Specialty Portfolio Specialist/Associate Portfolio Specialist, will demonstrate a sense of urgency to prepare and successfully execute a new product launch plan for their assigned geography. The Multi-Specialty Portfolio Specialist/Associate Portfolio Specialist, will drive results that are consistent with the company's goals, mission, and values.
Job Duties and Responsibilities
Deliver Results
* Consistently meet or exceed sales objectives by leading and implementing effective sales strategy in an ethical and compliant manner
* Demonstrates resilience and consistent ability overcome obstacles to achieve objectives
* Consistently demonstrate SMPA Values
Business Planning and Execution
* Develop and execute an effective business plan aligned to sales strategy to achieve sales results
* Prioritize and call on the appropriate customers at the optimal frequency to change prescribing behaviors
* Demonstrate effective pre-call planning prior to HCP engagement to establish a clear purpose for the sales call
Impactful Selling
* Move customers along the adoption continuum by driving market share growth
* Demonstrate two-way dialogue with customer interactions by employing selling skills to generate dialogue, identify customer needs and active listening
* Effectively utilize patient type selling with approved messaging and resources
Infinite Mindset
* Deploy growth mindset daily
* Focus on opportunities not limitations
* Expect success
Key Core Competencies
* Has a proven, consistent track record of exceeding sales goals in assigned geography or relevant experience.
* Proven to be successful in all aspects of selling, i.e., clinical expertise, selling skills, and an in-depth understanding of the local ecosystem or relevant experience.
* Understands, analyzes, and effectively presents scientific/technical details and marketing materials.
* Proficient knowledge and understanding of the payer landscape including commercial, Medicaid, and Medicare or relevant experience.
* Demonstrates the ability to analyze complex data to develop strategic and actionable business plans to deliver sales results.
* Candidates must have excellent communication & organizational skills and be proficient with technology platforms and business hardware/software.
Education and Experience
* Bachelor's Degree is required, preferably in Business or Life Sciences.
* Generally, the Associate Portfolio Specialist will require 0 - 3+ years of pharmaceutical sales experience and/or relevant experience. Demonstrated mastery or the aptitude to learn, product and disease state knowledge.
* Generally, the Portfolio Specialist will require 3 - 5+ years of pharmaceutical sales experience and/or relevant experience. Demonstrated mastery or the aptitude to learn, product and disease state knowledge.
* Travel within territory is required, which may include both car and overnight air travel depending upon territory.
* Some national travel to corporate headquarters, training, product theaters and sales meetings is required on a periodic basis.
* Work hours may include meetings scheduled outside of normal working hours.
The base salary range for the Associate role is $84,000 to $105,00. The base salary for the Portfolio Specialist is $108,000 - $135,000.00. Base salary is part of our total rewards package which also includes the opportunity for merit-based salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical, dental, vision, life and disability insurances and leaves provided in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays plus additional time off for a shut-down period during the last week of December, 80 hours of paid sick time upon hire and each year thereafter.
Total compensation, including base salary to be offered, will depend on elements unique to each candidate, including candidate experience, skills, education and other factors permitted by law.
Disclaimer: The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.
Confidential Data: All information (written, verbal, electronic, etc.) that an employee encounters is considered confidential.
Compliance: Achieve and maintain Compliance with all applicable regulatory, legal and operational rules and procedures, by ensuring that all plans and activities for and on behalf of Sumitomo Pharma America (SMPA) and affiliates are carried out with the "best" industry practices and the highest ethical standards.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Mental/Physical Requirements: Fast paced environment handling multiple demands. Must be able to exercise appropriate judgment as necessary. Requires a high level of initiative and independence. Excellent written and oral communication skills required. Requires ability to use a personal computer for extended periods of time.
Sumitomo Pharma America (SMPA) is an Equal Employment Opportunity (EEO) employer
Qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Auto-ApplyMedicaid Benefit Counselor (Part-time)
Saint Petersburg, FL job
Job Description
The ADRC serves elders aged 65 or older, adults aged 18-64 with a disability, and their caregivers. Staff support informed decision making, provide Medicaid eligibility assistance for the Statewide Medicaid Managed Care Long-term Care Program (SMMCLTCP), and provide the following duties and responsibilities through customer service that is streamlined, efficient, and consumer-friendly.
Duties and Responsibilities:
Medicaid Outreach and LTCPE, including:
Counsel individuals on the Statewide Medicaid Managed Care Long-term Care Program (SMMCLTCP), available services, eligibility requirements, the application process, and additional information sources.
Provide outreach that is standardized and consistent statewide to ensure public awareness of Medicaid programs and services and how to access them.
Build relationships with and educate service providers and other professionals to facilitate referrals and increase awareness of Medicaid resources.
Medicaid Eligibility Screening and Pre-enrollment (APCL/Waitlist) Placement, including:
Accept referrals from the ADRC Helpline and other sources for screening utilizing the DOEA approved 701S screening instrument.
Determine the individual's needs and enroll on the pre-enrollment list Waitlist (APCL/waitlist).
Ensure accurate data entry into eCIRTS , and SharePoint.
Inform individuals or individual's representatives about potential eligibility for the Medicaid programs, including their rights and responsibilities.
Re-evaluate individuals on the pre-enrollment list (APCL/waitlist) using the standardized screening instrument as required or as requested due to a significant change.
Enrollment Management System (EMS), including:
Provide the duties outlined in the most recent DOEA EMS release procedure.
Contact individuals on the release verbally and in writing.
Verify an individual's current Medicaid eligibility status.
Assist the client to pursue the eligibility process with meeting SMMCLTCP financial and medical eligibility.
Work with client to obtain the Physician Referral form (3008).
Coordinate with CARES (Comprehensive Assessment and Review for Long Term Care Services) staff for determination of medical eligibility.
Track Medicaid applications through the eligibility process.
Act as a consumer advocate by coordinating with CARES and DCF/ESS staff to resolve in a timely manner any eligibility issues that arise during the Medicaid eligibility determination process.
Assist clients who have lost Medicaid to regain their active status in SMMCLTCP.
Grievances and Complaints, including:
Provide assistance to SMMCLTCP enrollees, concerning how to file grievances and complaints with the long-term care plans.
Provide information concerning Medicaid Fair Hearings.
Maintain a record of such complaints, in accordance with statewide procedures.
Quality Assurance, including:
Assist with quality assurance reviews of 701S and long-term care education contacts by ADRC staff.
Assist with ensuring eCIRTS data integrity.
Assist with tracking and reviews of EMS processing to ensure contractual compliance.
Education:
Possess a bachelor's degree from an accredited college or university; or
Have an Associate of Arts Degree from an accredited college or university and a minimum of one year experience as a caseworker, case manager, intake specialist, or experience in performing human services related work; or
Have a high school diploma or GED and two years' experience as a caseworker, case manager, intake specialist, or experience in performing human services related work.
Skills/Qualifications:
Knowledge of computer applications to perform the functions of the position, including word processing, database, and spreadsheet applications.
The ability to work independently and with minimal supervision.
Knowledge of available ADRC administered programs and available Medicaid programs.
The ability to work with disabled adults, elders, caregivers, stakeholders, and community partners in a knowledgeable, engaged, and compassionate manner.
The ability to set and track personal performance goals to efficiently manage workload.
Special Requirements: Must pass DOEA Level II criminal background screening; must sign Medicaid Attestation Payroll Form per Department of Elder Affairs/AAAPP requirements. Must sign SMMCLTC Program - Prohibited Activities.
Equal Opportunity Employer:
At AAAPP, we take pride in providing equal employment opportunities to everyone regardless of their race, ethnicity, beliefs, religion, marital status, gender, citizenship status, age, veteran status, or disability. Accordingly, the purpose of this policy is to reinforce our commitment to the creation and maintenance of a diverse workplace where equality, respect, and consideration for one another are the norm.
Job Type: Part-time - 25 hours per week
Salary: $21 per hour
Benefits:
401(k)
401(k) matching
Paid time off
Education:
High school or equivalent (Required)
Experience:
Case management: 1 year (Required)
Schedule:
Flexible 5 hours daily - Monday to Friday
Work Location: Hybrid remote in Saint Petersburg, FL 33702
Associate Scientist - R&D
Plantation, FL job
Clinical Diagnostic Solutions, Inc. (CDS) is a company that provides total hematology solutions for the physician office laboratory, clinic, small hospital, and veterinary office markets. At CDS, our mission is to provide the highest quality experience to our valued customers. Our employees achieve this through our cultural goals of working together through Teamwork, high Quality in the work we do, being Innovative and Courageous, always Results Oriented, and most importantly - being Customer Oriented.
Under supervision, uses fundamental concepts, practices, and procedures of particular field of specialization to perform scientific, R&D tasks of some complexity requiring application and adaptation of established techniques, procedures, and criteria. Participates in new product development, optimization, validation, and transfer into production. Prioritizes work schedules to support team objectives.
Job Responsibilities:
Participates in method development and technical innovation within the research team and supports project timelines
Performs method optimizations, validations and participates in technology transfer to production
Performs routine operation, maintenance, calibration and troubleshooting of laboratory instruments such as pH, conductivity meters, osmometers, spectrnphotometers, hematology analyzers and nucroscopes
Evaluates and selects methods, applies protocols and scientific techniques to accomplish study objectives
Drafts and updates protocols, test methods and standard operating procedures as applicable
Proactively collaborates and supports the team, communicates problems as they arise
Provides solution/s to problem/ s of limited complexity, exercises judgment within defined policies to determine appropriate action
Collects, analyzes and compiles data. Summarizes for interpretation and discussion
Drafts statistical and narrative reports as applicable
Recognizes and reports experimental variances
Is able to coordinate a small project or a small component of a larger project according to set deliverables
Maintains good laboratory records and documentation for experimental work and results Maintains workplace safety and environmental practices
Maintains clean workplace including laboratory bench and glassware
Supports the department with QC technical investigation activities as needed
Works in the spirit of continuous improvement
Engages in inter and intra-departmental activities/studies Performs other related duties as required or as directed. The omission of specific duties does not preclude the supervisor from assigning duties that are logically related to the position.
Qualifications:
Knowledge of scientific approach and methodologies.
Ability to design small studies, gather, organize and analyze statistical data and generate reports
Excellent oral and written communication skills
Ability to investigate and analyze information and to draw conclusions
Skill in the use of personal computers and related software applications such as Word/Excel/Powerpoint/Teams
Knowledge of current technological developments/trends in area of expertise is desirable but not required
Capable of adjusting to dynamic work environment and changing priorities
Willing to take on new challenges and implement new ideas
Must be Comfortable handling blood products
Willing to embrace a learning environment, is open to suggestions, new ideas and innovation
Ability to grasp methods fast and willingness to change course as applicable
Familiar with GLP, GMP practices and capable of working in a regulated medical device company (ISO and FDA)
Must have strong analytical skills
Must be a team player and driven individual Must value innovation, accuracy and accountability
Minimum Requirements:
Bachelor's degree with 2-5 years or Associates degree with 5-8 years' experience that is directly related to the duties and responsibilities specified.
EOE
Veterinary Assistant
The Villages, FL job
Looking for a fulfilling career where you can make a real difference in the lives of pets and their owners? We are excited to announce the opening of the brand new Priority Pet Urgent Care state of the art clinic here in Wildwood! We'll be available for urgent care pet needs 4 pm - 12 midnight Monday - Friday and 10 am - 6pm Saturday & Sunday. We are eager and ready to serve the local community and their pets!
The Priority Pet Urgent Care mission is committed to providing easy-to-access quality care with a promise to our clients that their pets are our priority. We value teamwork, compassion, and excellence, offering a supportive work environment with opportunities for growth and development.
We look forward to connecting!
To learn more about us, please visit our website at ********************************
Job Description
Job duties include, but are not limited to:
Pet restraint, triage incoming patients, collection and analysis of lab samples, diagnostic imaging, management and nursing care of medical and hospitalized cases with varying degrees of stability, administration of medications, effective communication of treatment plans with clients, surgical preparation and assistance, and anesthetic management.
Must be able to withstand unpleasant odors and noises. May be exposed to bites, scratches, animal waste and potentially contagious diseases.
Whether you're looking to just be a master of your role or trying to grow into that next career move, you'll have opportunities through a variety of virtual and hands on, interactive training and continuing development.
Qualifications
We're looking for:
* An experienced Veterinary Assistant with a minimum of 1+ years professional experience.
* Compassionate, calm team player.
* Ability to multitask.
* Strong communication skills.
* Must be able to properly restrain pets.
* Proficient in sample collection, obtaining medical histories, processing laboratory tests and radiographs, and anesthesia monitoring are a bonus!
* Self-starter with the desire to continue to advance your knowledge and skillset.
Additional Information
We offer our staff:
* Comprehensive Benefits (health, dental, vision, liability, 401k & 401K matching program, life & supplemental insurance, HSA, & FSA)
* Employee Assistance Program
* Paid Vacation and Sick Time for ALL Employees
* Paid Bereavement Program
* Paid Parental Leave Program
* Competitive Compensation
* Continuing Education Allowance (applies to licensed/registered/certified roles)
* Tuition Assistance Program
* Access to a CVA/CVT/CVPM Partnership through Penn Foster
* Career Development Opportunities
* Referral Bonus Program for most positions!
* Additional Benefits May Also Be Available (i.e. Personal Pet Discounts, Holiday Pay, Uniform Allowance, Bonuses etc)
Hiring eligibility may be contingent to a candidate authorizing and completing a satisfactory background check.
* Note - some benefits may only be available to or vary slightly for full time employment status vs part time status.
For additional details including our full equal opportunity statement, texting/outreach communication authorization, physical requirements of the job and more, please visit: ***********************************************************