• Manufacturing Associate

    Kelly Services (Clearwater, FL)
    …product meets all acceptable criteria per SOPs + Following all FDA /CGMP regulations regarding traceability and safety procedures + Supporting, encouraging, and ... participating in team-related activities + Assisting in training manufacturing associates + Reporting unusual conditions and problems to supervisor and manufacturing lead + Practicing good housekeeping **This job might be an outstanding fit if you:** + Have a… more
    Kelly Services (01/14/26)
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  • Team Lead

    Charles River Laboratories (Raleigh, NC)
    …proudly supported the development of 86% of the drugs approved by the FDA in 2021. **Equal Employment Opportunity** Charles River Laboratories is an Equal ... Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. If you are interested in applying to… more
    Charles River Laboratories (01/14/26)
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  • Quality Technician 3

    ManpowerGroup (Newark, DE)
    …focus on analytical testing and instrumentation. + Knowledge of quality management systems, FDA , QSR, ISO, and IVDD standards. + Proficiency with MS Office, SAP, ... LIMS, and Siemens Clinical testing software. + Strong laboratory skills, including operation, maintenance, and troubleshooting of analytical instruments. + Excellent communication skills and the ability to work independently or as part of a team. **What's in… more
    ManpowerGroup (01/14/26)
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  • Customer Care - Product Technical Support…

    ZOLL Medical Corporation (Pittsburgh, PA)
    …Super Saturated Oxygen (SSO2) Therapy is the first FDA -approved therapy since the stent 20+ years ago to ... reduce infarct size in patients with the most severe heart attacks. Heart disease is the leading cause of death for both men and women in the US At ZOLL, your work will help to ensure cardiac patients get the life-saving therapy they need.ZOLL has been… more
    ZOLL Medical Corporation (01/14/26)
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  • New Patient Coordinator

    Penn Medicine (Philadelphia, PA)
    …standards and requirements, including TJC, Department of Health, funding agencies, FDA , HIPPA, HCFA, DPW, LCGME, SCGME, department specific guidelines and other. ... + Ensures patients have been properly registered and referred to Financial Counseling. + Makes sure new patients arrive for new patient appointment with referral and copays, as appropriate. + Maintains an excellent understanding of managed care plans and… more
    Penn Medicine (01/14/26)
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  • Associate Director, Clinical Science

    Bristol Myers Squibb (Princeton, NJ)
    …PowerPoint, etc.) as well as job-related programs such as SpotFire. + Knowledge of FDA , EMA and ICH regulations and guidelines a must. + Ability to effectively ... collaborate cross-functionally, across all levels of the organization. \#Rayzebio If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will… more
    Bristol Myers Squibb (01/14/26)
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  • Quality Rep

    BioLife Plasma Services (Worcester, MA)
    …highly desirable. Demonstrated understanding of quality assurance in an FDA -regulated environment. Demonstrated understanding of plasma center operations. Effective ... organizational, technical and problem-solving skills. Leadership Integrity Fairness Honesty Perseverance Putting the patient at the center Building trust with society Reinforcing our reputation Developing the business Decision-making and Autonomy Responsible… more
    BioLife Plasma Services (01/14/26)
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  • Senior Quality Manufacturing Engineer

    Cordis (Irvine, CA)
    …practices. + Audit Support: Support internal and external audits, including FDA inspections, by providing documentation, data, and expertise related to manufacturing ... quality. + Product Testing: Support and coordinate product testing, equipment qualifications, validation and verification processes to ensure required specifications are met. + Mentor and provide technical guidance to junior engineers, fostering their… more
    Cordis (01/14/26)
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  • Senior Manager Strategic Sourcing and Category…

    Abbott (Plymouth, MN)
    …chain solutions. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, ... and task assignments. + Able to build collaborative relationships with and influence a matrixed organization of R&D, NPI, Finance, PMO, Site SC, Manufacturing teams + Maintains positive and cooperative communications and collaboration with all levels of… more
    Abbott (01/14/26)
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  • Senior Process Manufacturing Engineer

    Steris Corporation (Atlanta, GA)
    …but not limited to, radioactive materials, licensing compliance, safety, EPA, OSHA, NFPA, FDA rules and regulations are adhered to. Maintains a working knowledge of ... regulations. The Experience, Skills, and Abilities Needed Required: + Bachelor's Degree in a technical discipline with minimum of 10 years' experience or minimum of 20 years' experience in lieu of degree + Minimum of 5 years of related experience in complex… more
    Steris Corporation (01/14/26)
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