• QA Documentation Control Specialist

    Astrix Technology (Rancho Dominguez, CA)
    …a culture dedicated to product consistency and customer satisfaction._ The ** Quality Assurance Documentation Specialist** is responsible for ensuring that all ... complies with regulatory requirements, food safety standards, and internal quality control procedures. **Pay rate:** $24- 25/ hr. **Location:** Compton,… more
    Astrix Technology (07/28/25)
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  • Sr. Staff Embedded Software Engineer

    Abbott (Alameda, CA)
    …the development, verification, ensuring timely delivery and adherence to FDA -compliant design control procedures. They provide technical leadership, mentoring, and ... and implement process improvements. Collaborating with cross-functional teams, they ensure high- quality software delivery and contribute to the full development life… more
    Abbott (07/14/25)
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  • Senior Embedded Software Engineer

    Abbott (Alameda, CA)
    …development, verification, and validation; responsible for on-time delivery of high- quality embedded software biowearable products that meet budgetary objectives. + ... approved design control procedures for software development in accordance with FDA guidelines. + Lead software development projects, providing mentoring and… more
    Abbott (06/07/25)
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  • Pharmacy Compliance Coordinator (Full-Time, 8-Hour…

    Stanford Health Care (Palo Alto, CA)
    …Ensures organizational compliance with federal/state regulations and accreditation requirements ( FDA , CDPH, BOP, TJC, etc.) for medication management. Develops audit ... Develops and contributes key performance indicator (KPI) data to the Pharmacy Quality Dashboard. Assist in maintaining dashboard. + Supports regulatory surveys and… more
    Stanford Health Care (08/17/25)
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  • Director, Product Security MedTech

    J&J Family of Companies (Irvine, CA)
    …Define and execute the product security strategy aligned with business priorities, FDA /MDR/524B expectations, and QMS requirements. + Lead and grow a global product ... devices, and cloud environments (AWS/Azure IoT). + Partner with Regulatory, Quality , Legal, Privacy, and Commercial teams to ensure cybersecurity requirements are… more
    J&J Family of Companies (08/28/25)
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  • Sr. Manager, Clinical Data Management

    Terumo Neuro (Aliso Viejo, CA)
    …and developing and/or enhancing data management processes to ensure complete, accurate, high quality clinical data and adhering to Good Clinical Practices and FDA ... as appropriate. + Assure regulatory compliance of vendors with company SOPs, FDA and ICH guidelines and other applicable regulations and guidelines. + Review… more
    Terumo Neuro (08/19/25)
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  • Supervisor, Manufacturing - (IGIV Filling) Swing…

    Grifols Shared Services North America, Inc (Los Angeles, CA)
    …and implement measures to improve production methods, equipment performance, facility layout, and quality of product. + Maintain a quality presence to ensure ... years of related experience in a pharmaceutical, GMP, or FDA regulated environment is required. + Equivalency: In lieu...years of related experience in a pharmaceutical, GMP, or FDA regulated environment. + Requires an in depth understanding… more
    Grifols Shared Services North America, Inc (07/25/25)
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  • Nurse Practitioner/Physician Assistant - Solid…

    Stanford Health Care (Palo Alto, CA)
    …has been in treating B-cell lymphoma, where CAR T-cell therapy has become an FDA -approved standard of care. We are now expanding our efforts to develop cell ... Ordering, Furnishing or Prescribing of Drugs; Formulary Protocol] Medications that are not FDA -approved or are used for a non- FDA - approved indication (off-label… more
    Stanford Health Care (07/08/25)
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  • RayzeBio Associate Director - Biostatistical…

    Bristol Myers Squibb (San Diego, CA)
    …+ Oversee vendors' activities, and review vendors' deliverables to ensure quality + Create/QC SDTM/ADaM data specifications, create/QC CDISC datasets and provide/QC ... clinical trial data and generating outputs to support DSUR/IBs, publications, FDA meeting briefing documents, and other internal ad-hoc requests + Collaborate… more
    Bristol Myers Squibb (08/30/25)
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  • Regulatory Affairs Manager

    Kelly Services (Valencia, CA)
    …for a leading client. In this role, you'll ensure compliance with FDA , ISO, and international regulations and submissions while managing regulatory programs across ... two facilities. **Key Responsibilities:** + Oversee regulatory submissions ( FDA , EU MDR, international). + Maintain product registrations, certifications, and export… more
    Kelly Services (08/16/25)
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