• Sr. Quality Engineer

    Envista Holdings Corporation (Pomona, CA)
    …Develops or participates in establishing requirements for all verification and validation (design and process) activities. + Apply state-of-the-art inspection and ... internal and external audits and inspections. + Maintains process and software validation plans. Writes validation protocols. Facilitates completion of … more
    Envista Holdings Corporation (06/13/25)
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  • Senior Quality Specialist, IVD

    Kelly Services (Sunnyvale, CA)
    …development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle ... guidance for Market Specification, Functional Specification, Design Verification, Design Validation , Test Method Validation , Risk Assessments, and Design… more
    Kelly Services (07/29/25)
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  • Software Quality Engineer II

    Abbott (Sylmar, CA)
    …R&D in the completion of system/software requirements and other verification and validation processes related to embedded software products. + Participate in reviews ... provide useful feedback. + Create and execute or direct software validation protocols traceable to system/software requirements. Execute and support on-time… more
    Abbott (07/03/25)
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  • Sr. Quality Specialist

    Danaher Corporation (Sunnyvale, CA)
    …development, specially design control and risk management activities in accordance with FDA and ISO regulations. This position is also responsible to apply ... guidance for Market Specification, Functional Specification, Design Verification, Design Validation , Test Method Validation , Risk Assessments, and Design… more
    Danaher Corporation (06/05/25)
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  • Sr. Manager, Clinical Data Management

    Terumo Neuro (Aliso Viejo, CA)
    …accurate, high quality clinical data and adhering to Good Clinical Practices and FDA regulations. Job duties: + Develop and implement SOPs to ensure GCP/ICH ... as appropriate. + Assure regulatory compliance of vendors with company SOPs, FDA and ICH guidelines and other applicable regulations and guidelines. + Review… more
    Terumo Neuro (05/20/25)
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  • Sr. Quality Engineer

    Abbott (Temecula, CA)
    …design change projects + Accountable for Design Verification and Validation planning & execution, including active cross-functional root-cause analysis investigation ... + Lead design test and inspection method development, and lead method validation activities + Ensure DHF content completion, integrity, and regulatory & standards… more
    Abbott (05/15/25)
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  • Test Engineer

    Actalent (Irvine, CA)
    …duties. Skills Test equipment, Labview, Software testing, Test engineering, Validation , Electrical engineering, Hardware Top Skills Details Test equipment, Labview, ... Software testing, Test engineering, Validation ,Electrical engineering, Hardware Additional Skills & Qualifications Design, fabricate, document, deploy and maintain… more
    Actalent (07/31/25)
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  • Medical Device Program Manager

    US Tech Solutions (San Bruno, CA)
    …device product development life-cycle, Risk Management, Design/Process Verification, and Validation . + Supporting product development through knowledge of Quality ... and US and International Medical Device Regulations & Regulatory Agencies (eg, FDA , Notified Bodies, etc.), and regulatory audits. + Performing product qualification… more
    US Tech Solutions (07/18/25)
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  • Scientist II, R&D Technical Business Solutions

    Fortive Corporation (Irvine, CA)
    …Scientist 2, R&D will use knowledge of scientific techniques to contribute to validation or qualification of external devices to be reprocessed in company products ... Performs various routine laboratory studies and assignments to support the validation and qualification of medical devices for reprocessing in ASP sterilization… more
    Fortive Corporation (06/12/25)
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  • System Administrator and Informatics Specialist

    Nestle (Los Angeles, CA)
    …the Vowst and Microbiome Sciences team with systems upgrades, computer system validation activities, and system administrative activities. This role is critical to ... in accordance with GxP, HIPAA, EU Annex 11, and FDA 21CFR Part 11 regulations. This role will also...ERP). * Collaborate with Information Technology (IT), Computer System Validation (CSV), and Quality Assurance Validation (QAV)… more
    Nestle (08/08/25)
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