• QC Supervisor

    BD (Becton, Dickinson and Company) (San Diego, CA)
    **Job Description Summary** Quality Control (QC) Supervisor is responsible for leading the day-to-day activities of the QC team. The supervisor should have a ... thorough knowledge of the various quality control processes including QC testing assays,...minimum of six years relevant technical experience within medical, pharmaceutical or Life Science industry. **Experience:** + A minimum… more
    BD (Becton, Dickinson and Company) (11/10/25)
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  • VSM Laboratory Manager (Biologics Industry)

    Fortive Corporation (Irvine, CA)
    …workflows. + Lead Lean projects aimed at enhancing operational efficiency, quality control , and overall productivity. + **Non-Conformance Processes Management:** ... audits, inspections, and documentation reviews to maintain regulatory compliance. + Implement quality control measures to ensure accurate and timely completion… more
    Fortive Corporation (10/15/25)
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  • Pharma Production Package Handler

    US Tech Solutions (South San Francisco, CA)
    …can work with a small team responsible for manufacturing custom shipping solutions, quality control of our current shipping solutions, and research and design ... to support a new project. **Responsibilities:** + Manufacture Custom Shipping Solutions. + Quality Control for our current packing and shipping protocols and… more
    US Tech Solutions (11/15/25)
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  • Manufacturing Engineer

    Hologic (San Diego, CA)
    …with cGMP regulations and guidelines related to plastics in the pharmaceutical or biotechnology industry. + Working knowledge of microprocessor controls, utility ... systems and process engineering + Biotech / Medical Device / Pharmaceutical industry experience + Thorough knowledge of manufacturing automation systems and… more
    Hologic (11/25/25)
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  • Principal Research Scientist II

    AbbVie (Irvine, CA)
    …of senior and principal scientists to ensure efficient day-to-day group operation; high- quality data generation and interpretation to drive the growing product and ... Qualifications: + BS, MS, or PhD in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biophysics or closely related field with typically 16+ (BS),… more
    AbbVie (11/25/25)
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  • Software Solution Program Management Lead

    Roche (Santa Clara, CA)
    …research and development teams along the sequencing datapath - instrument control , real time analysis, platform management, and downstream post-primary analysis ... business functions / partners. + You will ensure compliance with Roche processes, quality , and regulatory requirements. **This is an onsite position based in Santa… more
    Roche (11/12/25)
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  • HPLC Scientist III - R&D

    Kelly Services (Irvine, CA)
    …or verification protocols for API and drug product testing. + Collaborate with Quality Control to transfer methods and ensure accuracy and compliance. + ... seeking a **Scientist III** to join the **R&D team** at a leading pharmaceutical company in Irvine, CA. If you're passionate about advancing drug product development… more
    Kelly Services (11/12/25)
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  • Software Validation Specialist

    VTI Life Sciences (San Diego, CA)
    Quality Engineering, Automation and Validation Services to the Pharmaceutical , Biotechnology, Biologics and Medical Device industries. VTI offers professional ... and ambitious engineers looking to accelerate their career in the pharmaceutical , biotechnology and medical device industries. We offer an opportunity to… more
    VTI Life Sciences (11/07/25)
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  • Health Facilities Evaluator, Nursing

    The County of Los Angeles (Los Angeles, CA)
    …of Federal and State licensing and certification requirements relating to the quality of medical care. Health Facilities Evaluators generally are assigned to a ... of the facility being surveyed including physician, nursing, dietary, pharmaceutical , medical records documentation, social services, administrative management, ethical… more
    The County of Los Angeles (10/13/25)
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  • CMC Regulatory Affairs Senior/Consultant - Small…

    Parexel (Sacramento, CA)
    …and post-approval changes Cross-Functional Collaboration * Partner with manufacturing, quality , and external organizations to address CMC-related issues * Maintain ... is a plus * Ensure audit readiness and version control through meticulous documentation and system management Qualifications Experience...* 4-6 years of CMC regulatory experience in the pharmaceutical industry for a Consultant level role, 7+ years… more
    Parexel (10/11/25)
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