• Associate Director - Critical Utilities

    Takeda Pharmaceuticals (Thousand Oaks, CA)
    …The position requires establishing and executing a vision that prioritizes safety, quality , and continuous improvement. You will report into the Head of Engineering. ... of related experience. Experience in the pharmaceutical, biotechnology or other FDA -regulated industry strongly preferred + Minimum 5 years' experience in… more
    Takeda Pharmaceuticals (07/23/25)
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  • Ambulatory Clinical Pharmacist III

    Sutter Health (Oakland, CA)
    …in medical and departmental records as required. SAFETY. *Participates in quality improvement processes, including updating and revision of safety and procedure ... Security (DHS), Drug Enforcement Administration (DEA), Food and Drug Administration ( FDA ), and United States Pharmacopeia (USP). Possess written and verbal… more
    Sutter Health (07/23/25)
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  • Food Safety Specialist $70-$80k Quarterly Bonus…

    JBS USA (Manteca, CA)
    …and prerequisite program requirements. This position will ensure compliance to USDA/ FDA guidelines for food safety/SQF and BRC requirements. Also responsible for ... prerequisite compliance programs, manufacturing programs, customer requirements and other quality aspects through program management. **Responsibilities:** + Act as… more
    JBS USA (07/22/25)
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  • Principal Systems Engineer

    Abbott (Pleasanton, CA)
    …solutions to streamline product development in addition to ensuring product quality . Ensures the logical and systematic conversion of customer requirements and ... property. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes,… more
    Abbott (07/18/25)
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  • Cloud DevOps Engineer II

    Abbott (Sylmar, CA)
    …QA, and regulatory teams to ensure our systems are fast, reliable, and compliant with FDA and ISO standards. **What You'll Work On** As a DevOps Engineer 2 working ... releases. + Work with QA, regulatory, and external partners to bring high- quality , compliant software to market. Process and Compliance + Continuously improve our… more
    Abbott (07/18/25)
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  • Program Safety Lead, GPS Medical Science - Job ID:

    Ascendis Pharma (Palo Alto, CA)
    …appropriate representation during PV related regulatory inspections or internal quality assurance/corporate compliance audits. . Functions as a patient safety ... including a thorough understanding of PV processes + Expert knowledge of FDA , EMA PV regulations, ICH Guidelines, and other applicable regulatory guidance documents;… more
    Ascendis Pharma (07/17/25)
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  • Regional Sales Associate - Orange County/San Diego…

    Stryker (Sacramento, CA)
    …sales associated tasks, maintain strong, positive customer relationships, and to provide quality coverage in multiple territories across the country for employees on ... + Must adhere rigidly to all GMP policies and procedures as stipulated by the FDA . QUALIFICATIONS: + Must be able to handle routine overnight travel on short notice,… more
    Stryker (07/16/25)
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  • Counsel, Commercial - Heart Failure

    Abbott (Pleasanton, CA)
    …Claims Act, Civil Monetary Penalties Law, Stark, Beneficiary Inducement Statutes), FDA regulation (Food, Drug & Cosmetic Act), privacy (HIPAA), and anti-corruption ... Compliance, Finance, Education, Supply Chain, Research & Development, Regulatory, Quality , Clinical, Marketing, Commercial/Sales, and Information Technology Departments. +… more
    Abbott (07/15/25)
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  • Clinical Research Associate, Coronary (Remote)

    Cordis (Irvine, CA)
    …(Coronary)** role is a key position within the coronary program to help ensure FDA clearance through a PMA approval of this innovative device is granted and patients ... and Core Labs to ensure study operations and activities are of a high quality + Assist with organization and content preparation for Investigator meetings and Study… more
    Cordis (07/11/25)
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  • Staff Regulatory Affairs Specialist

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …with new and existing US and international regulations and directives (eg, FDA Medical Device Regulations, EU Low Voltage Directive, EU Electromagnetic Compatibility ... content. Support regulatory impact assessments for change controls and other Regulatory Affairs/ Quality Assurance items from a review and approval level. + Assist in… more
    BD (Becton, Dickinson and Company) (07/11/25)
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