• Warehouse Manager

    Gummi World (Chandler, AZ)
    Position Summary We are seeking a highly organized and structured Warehouse Manager with strong NetSuite ERP experience to lead daily warehouse operations in a ... discrepancies and implement corrective actions. + Ensure full compliance with cGMP, FDA requirements, and internal SOPs in all warehouse activities. + Maintain… more
    Gummi World (12/05/25)
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  • Sr. Manager , Design Assurance…

    Integra LifeSciences (Princeton, NJ)
    …outcomes and set new standards of care. **SUMMARY DESCRIPTION** The Senior Manager of the Tissue Technology (TT) Design Assurance Engineering department is ... + Participate in design and change control activities. + Participate in FDA inspections, ISO Certification and Surveillance audits and Internal audits. + Collaborate… more
    Integra LifeSciences (12/04/25)
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  • Donations Engagement Manager - Remote…

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …with raw materials or testing of raw materials that are included in FDA approved products/processes as well as with internal USP staff globally including: Program ... engaged, collaborative, and results-driven work environments The **Donations Engagement Manager ** has the following responsibilities: + Develops donation focused… more
    The US Pharmacopeial Convention (USP) (12/03/25)
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  • Quality Systems Manager

    Boar's Head Brand/Frank Brunckhorst Co., LLC (Holland, MI)
    …Essential Duties and Responsibilities + Assist in troubleshooting with USDA-FSIS and FDA regulatory issues and food safety or quality deviations. + Provide support ... manufacturing plants in the absence of the Senior Quality Manager + Responsible for communicating and working across all...Must be able to read and interpret FSIS and FDA regulations and required certification codes. Certificates, Licenses and… more
    Boar's Head Brand/Frank Brunckhorst Co., LLC (12/03/25)
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  • Food Safety and Quality Manager

    Kerry (Vesper, WI)
    …Develop, review and align procedures with Kerry global standards and FDA /CFIA expectations. Internally audit against global and regional standards and site ... and regulatory audit compliance. Support the site for regulatory inspections ( FDA /CFIA), identify preserved (ie.organic, Kosher) and customer audits. + Quality… more
    Kerry (12/03/25)
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  • Group Engineering Manager - Navigation…

    Globus Medical, Inc. (Methuen, MA)
    …We are seeking an experienced Systems Engineering and Hardware Systems Manager to lead a multidisciplinary team driving innovation in next-generation surgical ... transfer from R&D to production under ISO 13485 and FDA guidelines. + **Innovation & Continuous Improvement** + Identify...and real-time control systems are preferred + Knowledge of FDA 21 CFR Part 11, IEC 60601, and HIPAA… more
    Globus Medical, Inc. (12/03/25)
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  • Manager , IT Quality Engineering (LIMS)…

    Gilead Sciences, Inc. (El Segundo, CA)
    …to fulfil their aspirations. Join Kite and help create more tomorrows. **Job Description** ** Manager - LIMS Cell Therapy IT** We're here for one reason and one ... and approve LIMS system SOPs and reports per GMP, FDA , EU, Global, and ICH guidelines + Triage and...experience with SQL **Preferred Qualifications** + Strong understanding of FDA , ISO 13485, Medical Device Directive + Prior experience… more
    Gilead Sciences, Inc. (12/02/25)
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  • Pharmaceutical Audit Manager

    The Ritedose Corporation (Columbia, SC)
    The Audit Manager is responsible for the internal audit program, supplier quality management and coordination/execution of customer and regulatory audits. ... + ASQ Certified Quality Auditor required + Experience with FDA audits + Proficient with current word processing and...+ ASQ Certified Quality Auditor required + Experience with FDA audits + Proficient with current word processing and… more
    The Ritedose Corporation (11/22/25)
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  • Clinical Research Manager AI

    Dentsply Sirona (Charlotte, NC)
    …are listed in the United States on NASDAQ under the symbol XRAY. **Clinical Research Manager AI** Do you want to work with clinical studies in a world leading dental ... that are sufficient for ISO 14155, EU MDR and FDA . + Preparation and submission of clinical study documentation...of human clinical studies (eg ISO 14155, EU MDR, FDA , GDPR, Declaration of Helsinki, Good Clinical Practice (GCP)… more
    Dentsply Sirona (11/21/25)
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  • Sr. Manager , Human Factors and User…

    Takeda Pharmaceuticals (Lexington, MA)
    …work is done in compliance with IEC 62366 & regulatory body (example, FDA ) expectations. Drive HF/UX initiatives in early stage, development, and LCM projects, ... ensuring strategic and rigorous execution and timely delivery. **ACCOUNTABILITIES:** Senior Manager is responsible for Human Centered Design of Medical Devices and… more
    Takeda Pharmaceuticals (11/14/25)
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