• Quality Environmental Monitoring Specialist

    Actalent (Waukegan, IL)
    Job Title: Quality Environmental Monitoring Specialist Job Description We are seeking a motivated Quality Environmental Monitoring Specialist to join our team. ... our main Readycare division. You will play a crucial part in ensuring the quality and safety of our medical device and pharmaceutical products. Room for growth… more
    Actalent (09/09/25)
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  • Director, Regulatory Affairs and Quality

    Oura (San Francisco, CA)
    …product development, approval, and lifecycle management for all regulated features. + Ensure compliance with FDA , CE (MDR), and other relevant global regulatory ... We are looking for a Director, Regulatory Affairs and Quality Assurance to play a key role in shaping...wearables strongly preferred. + Proven track record of successful FDA submissions (510(k), De Novo) and international regulatory approvals.… more
    Oura (08/30/25)
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  • Food Safety Quality Assurance Technician

    Sysco (Dallas, TX)
    …**Education** + Formal job training in TQM principles, SPC, HACCP concepts, CFIA/ FDA regulations would be beneficial. + Formal quality and sensory ... fresh steaks and other meat, seafood and poultry, giving customers dependable quality , selection and freshness.** **BENEFITS** . Competitive pay . Ongoing job skills… more
    Sysco (08/27/25)
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  • Quality Operations Specialist

    Olon Ricerca Bioscience LLC (OH)
    …multiple documents simultaneously + Prepare and route documents for approval ensuring compliance with Good Documentation Practices (GDP) and FDA requirements + ... training to other team members as needed + Adhere to and ensure compliance with Quality System Standard Operating Procedures (SOP's), Good Manufacturing… more
    Olon Ricerca Bioscience LLC (09/03/25)
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  • Team Lead - Quality Control

    Globus Medical, Inc. (Eagleville, PA)
    …Summary** **:** The Team Lead is responsible for leading and assisting quality inspections and package testing on in-process materials and finished products. This ... not limited to, accurately completing all documentation and complies with applicable FDA , state, OSHA, AATB, and ISO regulations and standards. This individual works… more
    Globus Medical, Inc. (07/16/25)
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  • Associate Director, Regulatory/Scientific Affairs…

    Kemin Industries (Des Moines, IA)
    …global customers on regulatory and quality -related matters, and ensure the quality compliance of the business unit's product portfolio globally. We Are ... and within the business unit to assure regulatory and quality compliance for the products marketed and...to regulatory entities, including, but not limited to US FDA , EFSA, Health Canada, ANVISA, etc. + Responsible for… more
    Kemin Industries (09/12/25)
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  • Sr Manager - Quality Testing

    Mallinckrodt Pharmaceuticals (St. Louis, MO)
    … improvement and enhancement + Serve as the Subject Matter Expert during compliance audits + Study and improve various Quality processes through increased ... Job Title Sr Manager - Quality Testing Requisition JR000014963 Sr Manager - ...Summary Manage key product and stability testing groups and compliance activities to achieve site and corporate objectives. Specifically,… more
    Mallinckrodt Pharmaceuticals (08/22/25)
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  • Quality System Manager

    ThermoFisher Scientific (San Francisco, CA)
    …**Knowledge,** **Skills** **and Abilities:** + Exceptional cGMP, GLP and FDA compliance knowledge. + Possess a highly developed quality , regulatory and ... Systems aligning with Regulatory and Corporate Standards. Guide team to foster quality culture, compliance , and improvement. Lead team responsible for Document… more
    ThermoFisher Scientific (08/13/25)
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  • Associate Director, Clinical Program…

    Takeda Pharmaceuticals (Boston, MA)
    …my knowledge. **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring the compliance of ... and serious breach. This position supports Takeda's mission by maintaining high standards of quality and compliance in clinical trials. **This role is located in… more
    Takeda Pharmaceuticals (07/16/25)
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  • QA Specialist

    Actalent (Vista, CA)
    …aspects of the company. This includes the development and maintenance of the Quality Management System, obtaining FDA and ISO certifications, and product ... Quality System. + Conduct internal audits to ensure compliance . + Receive, review, and respond to customer product...quality supplements, annual reports, control documents, etc. to FDA authorities. + File Vigilance Reports or Medical Device… more
    Actalent (09/03/25)
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