• Geosyntec Consultants, Inc. (Boston, MA)
    …work environment. (required) Prior consulting or industry experience in medical device field, including managing projects with multiple staff. (preferred) ... Overview Gradient, a Geosyntec Company, is seeking a Senior Medical Device Toxicologist to assist colleagues and clients in toxicological risk assessments and… more
    Upward (07/02/25)
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  • Cognizant Technology Solutions (Chicago, IL)
    …Global Pharmaceutical market and industry, including BioTech, Medical Device , Traditional Rx, enabling technologies and regulatory /compliance in the ... Experience Partner - Life Sciences (Pharma / BioTech / Medical Device ) Associate Director - Chicago/Midwest Remote...to plan and run existing clients. You'll work with Consulting and other parts of Cognizant like Data, and… more
    Upward (07/16/25)
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  • Dawar Consulting, Inc. (Pleasanton, CA)
    medical engineering or Bio-engineering *0-3 years of industry experience *Preferred - Medical device experience Company Benefits: Medical , Dental, Vision, ... to support system verification and validations, and compile content for regulatory submissions. *With guidance, analyzes and brainstorms alternative approaches to… more
    Upward (07/03/25)
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  • DHD Consulting (Monroe, GA)
    …Position Summary Experienced Quality Assurance professional with 5-7 years in the medical device industry, focused on audit response, CAPA, validation, and ... - Minimum of 57 years experience in Quality Assurance within the medical device or pharmaceutical industry, including audit preparation, nonconformance handling,… more
    Upward (07/04/25)
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  • Pharmavise (Indianapolis, IN)
    …a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become ... Job Description Overview: From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to… more
    Upward (07/06/25)
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  • Pharmavise (Lebanon, PA)
    …a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become ... Job Description Overview: From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to… more
    Upward (07/23/25)
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  • VTI Life Sciences (San Diego, CA)
    …engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support ... Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training,… more
    Upward (06/29/25)
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  • Associate Director, Engineering - Medical

    Merck (Wilson, NC)
    …supporting regulatory inspections. + Experience in commercialization of high-volume medical device or combination products + Experience with injection ... the Wilson Packaging Technical Operations Team. This role will serve as the primary medical device and combination product (MDCP) point of contact for the site… more
    Merck (07/23/25)
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  • Project Engineer (Med Device )

    Element Materials Technology (Fairfield, OH)
    **Overview** Element has an opportunity for an *on-site* ** Medical Device Project Engineer** to join our rapidly expanding team in Fairfield, Ohio. This position ... scheduling, testing , data analysis and reporting. The Project Engineer will manage medical device testing projects, using standard and custom test frames across… more
    Element Materials Technology (06/19/25)
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  • Moment - Experience Partner - Life Sciences…

    Cognizant (Chicago, IL)
    …Global Pharmaceutical market and industry, including BioTech, Medical Device , Traditional Rx, enabling technologies and regulatory /compliance in the ... **Experience Partner - Life Sciences (Pharma / BioTech / Medical Device )** **Associate Director - Chicago/Midwest Remote**...to plan and run existing clients. You'll work with Consulting and other parts of Cognizant like Data, and… more
    Cognizant (07/11/25)
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  • Sr. Consulting /Principal Full Stack…

    RELX INC (Horsham, PA)
    …projects within LexisNexis Reed Tech Life Sciences. Our focus includes our cutting-edge medical device and drug product platforms, along with their ancillary ... a part of RELX, is a leading global provider of legal, regulatory , and business information. We help customers increase productivity and improve decision-making… more
    RELX INC (06/14/25)
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  • Director, Cybersecurity Regulatory Affairs

    IQVIA (Washington, DC)
    …guidelines, and apply these to services provided. * Stay current on US medical device regulatory requirements. Qualifications: * Bachelor's degree required; ... years of consulting or client facing experience preferred; direct healthcare and/or medical device experience preferred. * Should understand medical more
    IQVIA (07/10/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Boston, MA)
    …+ Bachelors in related field, preferred + 2+ years' experience in Medical Device Regulatory Affairs/Quality experience preferred + Certification ... Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to… more
    Cardinal Health (07/09/25)
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  • Senior Associate, Regulatory Operations

    Publicis Groupe (New York, NY)
    …Saatchi & Saatchi Wellness has provided consumer and professional marketing, strategic consulting , and medical education to pharmaceutical and wellness brands. ... submissions follow the protocols established by our pharmaceutical and medical /surgical device clients for promotional materials. This includes knowing… more
    Publicis Groupe (06/12/25)
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  • Post Market Surveillance Analyst III

    Abbott (Burlington, MA)
    …various types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global ... + 5 years related work experience **Preferred Qualifications** + 3+ years in MDR ( Medical Device Reporting) + Knowledge of the use, development, and … more
    Abbott (07/11/25)
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  • Lead Statistician

    Cook Medical (Bloomington, IN)
    …in experimentation and foster a culture of statistical rigor in our medical device development and manufacturing environments. Responsibilities + Lead ... initiatives, and collaborate across global teams to uphold Cook Medical 's commitment to quality excellence and regulatory ...testing , and method validation + Strong knowledge of medical device regulations (ISO 13485, 21 CFR… more
    Cook Medical (07/16/25)
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  • Director, Human Factors Engineering…

    Gilead Sciences, Inc. (Foster City, CA)
    …communication skills are required. + Demonstrated ability to facilitate the interface with medical device vendors and HF consulting firms. + Demonstrated ... aspirations. Join Gilead and help create possible, together. **Job Description** The Device , Packaging and Process (DPP) function is a key component of Gilead's… more
    Gilead Sciences, Inc. (06/24/25)
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  • Managing Consultant - Life Sciences Advisory…

    Guidehouse (Chicago, IL)
    …Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle ... value, access, pricing and commercialization strategy projects for pharmaceutical, biotechnology, medical device , and diagnostics companies. Our client services… more
    Guidehouse (07/03/25)
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  • Senior Manager, Global Design Assurance

    embecta (Parsippany, NJ)
    …Quality, the Sr. Manager of Design Assurance, will lead and build a dynamic medical device design assurance team focused on standardizing and deploying best in ... class processes that include the design and development of embecta's diabetes care medical device worldwide. This person will lead the engagement and interaction… more
    embecta (07/12/25)
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  • Biomedical Engineer

    Veterans Affairs, Veterans Health Administration (Prescott, AZ)
    …and preventive maintenance procedures as required. coordinates and assists with medical device hazard investigations to assure compliance with patient ... Incumbent provides engineering review, guidance, and development of the Medical Equipment Management Program encompassing professional engineering consulting...safety goals, Safe Medical Device Act (SMDA), and TJC requirements.… more
    Veterans Affairs, Veterans Health Administration (07/13/25)
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