• Aerospace Quality Engineer (Arp4754 / APQP / NPI)

    Safran (Irvine, CA)
    …and processes in accordance with ARP-4754A and other applicable industry and regulatory standards. The AQE ensures effective implementation of the program plan and ... full compliance of customer, regulatory and company requirements, to achieve company business objectives on all activities performed by the engineering organization.… more
    Safran (06/05/25)
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  • CRA 2 - Oncology, US East Coast, Central or West…

    IQVIA (San Francisco, CA)
    …work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines * Work with sites to adapt, ... regulatory requirements (ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). * Good therapeutic and protocol… more
    IQVIA (05/27/25)
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  • Senior Water/Wastewater Services Worker…

    Ventura County (Ventura, CA)
    …making process control adjustments as needed to ensure compliance with regulatory agencies and permit requirements; coordinating system maintenance functions, system ... to the department; ensures compliance with all federal and state regulatory requirements; resolves problems in treatment plants, collection systems, lift stations… more
    Ventura County (05/19/25)
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  • Principal Biologist

    Stantec (San Diego, CA)
    …Biologist, you will oversee and provide expertise in field biology, regulatory strategy, CEQA/NEPA analysis, and permitting strategy. Specific background and ... of excellent botanical, wetland, or wildlife technical expertise, expertise with regulatory permitting, and proven success in project and client management. This… more
    Stantec (08/07/25)
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  • Executive Director, Commercial Manufacturing

    Sumitomo Pharma (Sacramento, CA)
    …Team. + Collaborate with the process and analytical development, quality, and regulatory functions to establish a robust, compliant clinical supply chain to support ... company objectives. + Champion regulatory and technical documents for regulatory submissions...and external partners. + Available to travel domestically and international if/when needed. **Education and Experience** + PhD or… more
    Sumitomo Pharma (08/02/25)
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  • Supply Planning Specialist

    Interstate Blood Bank (Vista, CA)
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global ... have an extensive knowledge of complex blood and plasma processing, market and regulatory requirements, and be able to analyze and offer contingency plans when… more
    Interstate Blood Bank (08/02/25)
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  • Plant Manager

    BD (Becton, Dickinson and Company) (Milpitas, CA)
    …environment to drive continuous process and cost improvement, innovation, quality/ regulatory compliance, and development of team members through engagement, coaching ... environment to drive continuous process and cost improvement, innovation, quality/ regulatory compliance, and development of team members through engagement, coaching… more
    BD (Becton, Dickinson and Company) (07/30/25)
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  • RayzeBio Director, Medical Affairs Research…

    Bristol Myers Squibb (San Diego, CA)
    …will work cross-functionally with several departments (Clinical Operations, CMC, Regulatory Affairs, Supply Chain, Drug Safety/PV, Compliance and Legal). ... area oversight to ensure quality of work and appropriate compliance with regulatory requirements + Conduct budget negotiations for Medical Affairs IITs, including… more
    Bristol Myers Squibb (07/25/25)
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  • Clinical Development Program Lead, Neuropsychiatry…

    Bristol Myers Squibb (San Diego, CA)
    …trials and will supervise and have accountability for the clinical components of regulatory filings + Will contribute to overall strategy for specific disease / ... and Communication + Will work closely with colleagues in BMS Research, Development, Regulatory , Medical, Commercial and other key functional areas on a global basis;… more
    Bristol Myers Squibb (05/21/25)
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  • Principal Quality Mfg Engineer, Selution

    Cordis (Irvine, CA)
    …at every stage of the manufacturing process, ensuring compliance with regulatory standards and internal quality requirements. + Process Improvement: Lead the ... mitigation to ensure the safety and efficacy of medical devices. + Regulatory Compliance: Stay up-to-date with regulatory requirements, standards, and guidelines… more
    Cordis (05/15/25)
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