• Senior Privacy Engineer and Compliance Manager

    Abbott (Alameda, CA)
    …Global Privacy Officer for ADC, this role is responsible for supporting the review and design of privacy and compliance controls, mechanisms and protocols across the ... colleagues to ensure that the data processing meets established regulatory compliance needs. + Collaborate with product and system...new privacy products and features, as well as the review of in place products and technology to ensure… more
    Abbott (06/21/25)
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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). ... to ensure quality of work and appropriate compliance with regulatory requirements + Conduct budget negotiations for Medical Affairs...for all study related items. Create process for internal review of budgeting of trials + Maintain all internal… more
    Bristol Myers Squibb (08/17/25)
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  • Clinical Scientist II

    Abbott (Santa Clara, CA)
    …to execution by working collaboratively with biostatistics, medical affairs, regulatory affairs, global clinical operations, and other cross-functional team members. ... The individual will also be interacting with regulatory agencies, reimbursement agencies and clinical trial investigators to ensure successful execution of clinical… more
    Abbott (08/16/25)
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  • Senior Director, Software Engineering

    Abbott (Pleasanton, CA)
    …Institute efficient communication and cross-functional collaborations with marketing, quality, regulatory , clinical, project management, etc, at multiple levels. + ... Interfaces with appropriate internal and external stakeholders ( regulatory , customers, etc.) to ensure development programs meet regulatory and customer… more
    Abbott (08/14/25)
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  • Mid-level Biologist

    AECOM (San Diego, CA)
    …candidate will have:** + Strong working knowledge of environmental regulatory requirements for projects in California. + Strong interpersonal, organizational, ... Experience working with design teams to avoid, minimize and streamline environmental regulatory permitting. + Ability to apply acquired expertise and knowledge to… more
    AECOM (08/13/25)
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  • Business Information Security Officer

    Coinbase (Sacramento, CA)
    …infrastructure and controls to protect critical business assets and meet regulatory compliance requirements * Lead engineering build activities for custom security ... functions require in-house capabilities versus outsourced solutions to meet local regulatory and business needs * Develop and maintain security policies, risk… more
    Coinbase (08/09/25)
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  • Quality Engineer II

    CTG (Woodland, CA)
    …Engineer II will develop and support all Quality Management System (QMS) and Regulatory Affairs (RA) activities in alignment with site quality goals and metrics. ... is responsible for new product setup, quality project management, and ensuring regulatory compliance for serum products. The position will ensure compliance with… more
    CTG (08/09/25)
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  • Senior Process Development Engineer

    Amgen (Thousand Oaks, CA)
    …process technology transfer and other technical documents. **Process Validation & Regulatory Support** + Development of validation plans and supports execution of ... + Ensure site's process validation business process adheres to global regulatory agency standards, Amgen's quality requirements, other site policies and procedures,… more
    Amgen (07/31/25)
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  • Product Manager

    Insight Global (San Jose, CA)
    …Engineering, and Product teams to design solutions that transform complex regulatory mandates into clear, scalable metrics reporting products and processes. ... Own and drive the roadmap for key product experiences, ensuring that regulatory and compliance needs are fully addressed. Translate legal and policy requirements… more
    Insight Global (07/26/25)
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  • Quality Compliance Specialist

    Adecco US, Inc. (Cupertino, CA)
    …in medical device labelling and a solid understanding of domestic and international regulatory requirements, including 21 CFR 801 and EU MDR. This role requires ... exceptional technical writing skills, regulatory awareness, and the ability to manage multiple projects...(IFU) in compliance with global medical device regulations + Review and manage marketing claims and post-market materials for… more
    Adecco US, Inc. (07/24/25)
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