• Sr. Supplier Quality Engineer I

    Integra LifeSciences (Princeton, NJ)
    …teams to ensure sterilization processes are integrated into the overall supplier quality process. ** Regulatory Compliance & Documentation:** + Ensure thorough ... of care. This position is for a Sr. Supplier Quality Engineer l - Global Supplier Quality ...meet organizational goals and objectives. + Experience with External Regulatory Agency audits (ie, Notified Bodies and FDA more
    Integra LifeSciences (06/06/25)
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  • Sr. Design Quality Engineer I

    Integra LifeSciences (Princeton, NJ)
    …and manage time to meet organizational goals and objectives. + Experience with External Regulatory Agency audits (ie, Notified Bodies and FDA ). + This position ... standards of care. This position is for a Design Quality Engineer Il with hands-on experience and proven success...such as ISO 13485, ISO 11135, ISO 11137, and FDA requirements. **Cross-Functional Collaboration:** + Work closely with sterility… more
    Integra LifeSciences (06/11/25)
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  • Executive Director of R&D Global Quality

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …Summary** We are seeking an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will be responsible for leading a ... global team focused on R&D Quality . This global role includes direct reports in the...submission support, lead the R&D audit program, engage with regulatory authorities, and maintain clinical data integrity. The leader… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Specialist, Quality Assurance - Individual…

    Actalent (Mahwah, NJ)
    …changes in accordance with Stryker's change management procedures and relevant regulatory requirements for medical devices. Key areas of responsibility * Facilitate ... business activities while remaining compliant with applicable internal and external regulatory requirements including but not limited to Site, Division, Corporate, … more
    Actalent (08/13/25)
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  • Quality Control Inspector I, 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …pathways to advance patient outcomes and set new standards of care. The ** Quality Inspector I** will be responsible for performing quality assurance inspections ... on purchased components, manufactured sub-assemblies and final product. The Quality Inspector will perform all duties in accordance to the requirements of overall… more
    Integra LifeSciences (06/16/25)
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  • Quality Control Inspector I, 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …pathways to advance patient outcomes and set new standards of care. The ** Quality Inspector I** will be responsible for performing quality assurance inspections ... on purchased components, manufactured sub-assemblies and final product. The Quality Inspector will perform all duties in accordance to the requirements of overall… more
    Integra LifeSciences (08/08/25)
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  • Quality Control Inspector I - 1st shift

    Integra LifeSciences (Plainsboro, NJ)
    …pathways to advance patient outcomes and set new standards of care. The ** Quality Inspector I** will be responsible for performing quality assurance inspections ... on purchased components, manufactured sub-assemblies and final product. The Quality Inspector will perform all duties in accordance to the requirements of overall… more
    Integra LifeSciences (07/24/25)
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  • Pharmaceutical Quality Engineer

    Kelly Services (Somerset, NJ)
    ** Quality Validations Engineer- Somerset NJ** **Summary of Essential Functions:** The Quality Applications Engineer is tasked with supporting, maintaining, and ... optimizing digital quality systems and applications across the organization. This role...-related software tools are effectively implemented and aligned with regulatory requirements and business needs. The engineer collaborates with… more
    Kelly Services (08/14/25)
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  • Quality Assurance Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …advance patient outcomes and set new standards of care. **SUMMARY DESCRIPTION** The ** Quality Assurance Engineer II** will provide Quality compliance support on ... all aspects of the Plainsboro, NJ CMC Quality System. The Quality Assurance Engineer II...the Canadian Medical Device Regulations (CMDR), and other applicable regulatory agencies. The QA Engineer II will collaborate with… more
    Integra LifeSciences (05/18/25)
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  • Quality Associate

    Actalent (Basking Ridge, NJ)
    Job Title: Quality Associate Job Description The Quality Associate will work closely with the QA team and is responsible for maintaining all labeling files in ... internal procedures. The role involves coordinating labeling projects to ensure regulatory compliance and providing guidance to team members on labeling regulations… more
    Actalent (08/13/25)
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