• Geosyntec Consultants, Inc. (Seattle, WA)
    …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 (07/03/25)
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  • ProPharma Group (Western Springs, IL)
    … solutions that de-risk and accelerate our partners' most high-profile drug and device programs. The Associate Director, Principal Medical Writer II is ... document standards. Mentors less experienced writers. Reports to a Director of Medical Writing or above. Essential Functions: *Develop regulatory documents for… more
    Upward (06/29/25)
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  • ProPharma Group (Western Springs, IL)
    … solutions that de-risk and accelerate our partners' most high-profile drug and device programs. The Medical Promotional Review Consultant is responsible for: ... with relevant clinical data, publications, and treatment guidelines published by medical associations. Monitor US regulatory promotional environment by staying… more
    Upward (07/13/25)
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  • ProPharma Group (Western Springs, IL)
    …of patients by providing advice and expertise that empowers biotech, med device , and pharmaceutical organizations of all sizes to confidently advance scientific ... across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, … more
    Upward (07/03/25)
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  • Infosys (Chicago, IL)
    …ecosystems. This is to bring innovative medical devices and Software as Medical Device applications into the market to improve patient care while reducing ... Sciences - EM - Job Description: Infosys seeks a Client Partner for our Medical Devices and Life Sciences vertical. The person will lead all client interfaces within… more
    Upward (07/18/25)
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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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  • Exponent Inc. (Philadelphia, PA)
    …specific projects related to a variety of mechanical engineering applications including medical device and consumer product testing in the laboratory Designing ... About Exponent Exponent is the only premium engineering and scientific consulting firm with the depth and breadth of expertise to solve our clients' most profoundly… more
    Upward (07/01/25)
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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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  • Mechanical Engineer- R&D, Medical

    Eliassen Group (Marlborough, MA)
    …with CAD tools (SolidWorks preferred) . Familiarity with document control systems and regulatory documentation processes ( medical device experience a plus) . ... **Mechanical Engineer- R&D, Medical Device ** **Marlborough, MA** **Type:** Contract..._About Eliassen Group:_ _Eliassen Group is a leading strategic consulting company for human-powered solutions. For over 30 years,… more
    Eliassen Group (07/25/25)
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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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  • 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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