• Senior Analyst, QC, US Site (Hopewell, NJ)

    BeOne Medicines (Pennington, NJ)
    …and release of materials, intermediates and finished products under FDA /EU regulations, applicable International Regulations, BeOne processes and procedures. ... the Chemistry laboratory. This position reports to the QC Manager and is located full time at the Hopewell,...Minimum of 4+ years of working experience in an FDA -regulated biotechnology, pharmaceutical company are required. + Familiar with… more
    BeOne Medicines (01/06/26)
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  • Customs Specialist - Second Shift

    Kuehne+Nagel (Plymouth, MI)
    …customs entry transactions. Additionaly perform any tasks which are assigned by the Manager or Supervisor that meets and supports the needs of the Customs Brokerage ... Customs & Border Protection; PGA's (Participating Governmental Agencies ie FDA , EPA, DOT, FCC, Fish and Wildlife ) **How...+ Accurate completion of all PSG data interfaces (ie FDA , EPA, DOT, FCC, Fish & Wildlife etc )… more
    Kuehne+Nagel (01/02/26)
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  • Senior Process Engineer II - Endotoxin

    Integra LifeSciences (Princeton, NJ)
    …in compliance with industry standards. + Support the Environmental Controls Senior Manager with providing direction to the team, coordinating workflow, and providing ... ANSI/AAMI ST72, ISO 11737-3, USP <85>, USP <161>, and FDA guidelines. + Ensure proper integration of endotoxin testing...ANSI/AAMI ST72, ISO 11737-1, USP <85>, USP <161>, and FDA guidelines. TOOLS AND EQUIPMENT USED + Knowledge of… more
    Integra LifeSciences (01/02/26)
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  • Repair Technician - Bilingual

    Adecco US, Inc. (Union City, CA)
    …along with other tasks as requested by the department supervisor or manager . This role requires clear knowledge of quality processes, specifically working within ... an **ISO 13485 and FDA regulated environment** . This position focuses heavily on...devices. 3. Technical experience, preferably in a **regulated environment** ( FDA , ISO 13485, etc.), that includes engineering drawings and/or… more
    Adecco US, Inc. (01/01/26)
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  • Analytical Laboratory Supervisor (3rd shift)…

    Abbott (Sturgis, MI)
    …responsibilities; share accountability for line budgetary decisions with direct manager . Track, trend, and continuously improve budgetary performance for ... are followed You'll be accountable for meeting our compliance standards including FDA , OSHA and Abbott policies and procedures. **Required Qualifications** + High… more
    Abbott (12/31/25)
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  • Clinical Research Coordinator III - RN

    ThermoFisher Scientific (Frederick, MD)
    …collection procedures to ensure uniformly high levels of compliance with GCP, GLP, FDA and other government- or locally required guidance. + Relies on experience and ... years of experience in clinical research coordination, with expertise in FDA -regulated trials. + Experience utilizing clinical trial management systems and databases… more
    ThermoFisher Scientific (12/31/25)
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  • Maintenance Supervisor - Day Shift

    Abbott (Casa Grande, AZ)
    …of millions worldwide. You'll be accountable for meeting our compliance standards including FDA , OSHA and Abbott policies and procedures. **What You'll Work On** + ... and growth planning. + Follows escalation reporting process with inputs from peers/ manager for decision making as required. Make and communicate decisions that are… more
    Abbott (12/30/25)
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  • Director, Strategic Clinical Development

    United Therapeutics (Research Triangle Park, NC)
    …pulmonary arterial hypertension ( **PAH** ). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung ... inception (Phase 1-3) to successful product approval by the FDA and other regulatory agencies. + Design and review...and presentation) + Ability to thrive as both a manager and a team member + Ability to simultaneously… more
    United Therapeutics (12/26/25)
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  • Product Complaints Engineer

    DEKA Research & Development (Manchester, NH)
    …Device Research and Development environment. The position reports to the Product Complaints Manager . This is a high visibility role with a significant direct impact ... meets QMS requirements; and complies with US Food and Drug Administration ( FDA ) regulations / other regulatory requirements. + Identify and make sound decisions… more
    DEKA Research & Development (12/25/25)
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  • Customs Specialist

    Kuehne+Nagel (Seatac, WA)
    …customs entry transactions. Additionaly perform any tasks which are assigned by the Manager or Supervisor that meets and supports the needs of the Customs Brokerage ... Customs & Border Protection; PGA's (Participating Governmental Agencies ie FDA , EPA, DOT, FCC, Fish and Wildlife ) **The...+ Accurate completion of all PSG data interfaces (ie FDA , EPA, DOT, FCC, Fish & Wildlife etc )… more
    Kuehne+Nagel (12/25/25)
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