• Sr. Manager, Software Engineering

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …and quality . + Collaborate closely with product management, hardware engineering, quality assurance, and regulatory affairs teams to ensure alignment and ... software development teams in the medical device industry, with a strong understanding of regulatory requirements (eg, FDA 21 CFR Part 820, IEC 62304). +… more
    BD (Becton, Dickinson and Company) (12/25/25)
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  • Infusion Clinical Pharmacist, Oncology

    Sutter Health (Santa Cruz, CA)
    …at external facilities, and in the community to provide seamless and integrated quality care + Performs one or more of the following: + Second-level controlled ... requirements with ability to optimize procurement strategies while meeting regulatory requirements + Analyze reports/processes and the administrative functions… more
    Sutter Health (12/23/25)
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  • Director, Engineering

    Merck (West Point, PA)
    …life while ensuring compliance with FDA , EMA, and other regulatory requirements. + Collaborate closely with Quality Assurance, Validation, Manufacturing, ... teams. + Strong knowledge of pharmaceutical manufacturing processes, equipment, and regulatory requirements ( FDA , EMA, GMP). + Expertise in reliability… more
    Merck (12/20/25)
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  • Sr. Manager, Distribution Operations - Diagnostics

    Abbott (North Chicago, IL)
    …(WMS), inventory control, and transportation logistics. + Strong knowledge of healthcare regulatory & Transportation requirements ( FDA , GMP, GDP, IATA, DOT) + ... safety, and people leadership with fostering a culture of Quality , Safety, employee engagement and continuous improvement. **Responsibilities** + **Operational… more
    Abbott (12/12/25)
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  • Project Engineer

    Globus Medical, Inc. (Audubon, PA)
    …to ensure timely completion of tasks while remaining in full compliance with Globus quality system and other applicable regulatory bodies + Designs and develops ... sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our...and market plans + Assists in the writing of regulatory applications to the FDA and other… more
    Globus Medical, Inc. (12/01/25)
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  • Shift Supervisor Blood Bank - Day Shift

    Stony Brook University (Stony Brook, NY)
    …with applicable FDA , NYSDOH, AABB, CAP requirements and other relevant regulatory agencies requirements. + Assists all areas of the hospital in the interface ... the ED, OR and ICUs as well as IT, Clinical Informatics and Quality Assurance functions. The responsibilities of the TH Clinical Laboratory Technologist I include:… more
    Stony Brook University (11/26/25)
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  • Sales Support Administrator (Quoting Specialist)

    Element Materials Technology (Acton, MA)
    …and technical requirements. + Interpret and communicate complex testing protocols, regulatory requirements ( FDA , ISO/IEC 17025), and client specifications to ... **Overview** Join Element's **Santa Fe Springs laboratory** , an FDA -registered, ISO/IEC 17025-accredited facility specializing in **pharmaceutical testing, trace-metal… more
    Element Materials Technology (11/20/25)
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  • Senior Controls Engineer

    Abbott (Sylmar, CA)
    regulatory requirements. *Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating ... and process development from concept through sustained manufacturing of FDA regulated products. Responsible for production support, maintenance support, performing… more
    Abbott (10/16/25)
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  • Associate Director, Biostatistics

    CSL Behring (King Of Prussia, PA)
    …including integrated analyses for submissions. + Represent Biostatistics in interactions with regulatory authorities (eg, FDA , EMA, PMDA) + Be responsible for ... program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the… more
    CSL Behring (11/26/25)
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  • Senior Medical Writer, Clinical Evaluation…

    Abbott (Maple Grove, MN)
    …and supporting CER related projects and processes. + Supports additional clinical, regulatory , quality and engineering related deliverable as assigned. + ... Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality Engineering, Clinical Affairs, Clinical Science, Risk Management and Medical… more
    Abbott (12/20/25)
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