• Partner, Life Sciences Advisory

    Guidehouse (New York, NY)
    …Guidehouse Consulting Health Care Practice. Our clients include - pharmaceutical, biotechnology, medical device , drug delivery and diagnostic. Examples of ... reflects our commitment to creating a diverse and supportive workplace. Benefits include: + Medical , Rx, Dental & Vision Insurance + Personal and Family Sick Time &… more
    Guidehouse (05/22/25)
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  • Senior Quality Engineer

    Sanofi Group (Swiftwater, PA)
    …+ 3+ years of medical device industry experience + Experience in Medical Devices and/ or Drug Device Combination product development (eg ISO11608, ... Single Point of Contact (SPOC) for manufacturing sites of medical devices or combination products for device ...of medical devices or combination products for device related Change Controls topics. **Provide mentoring support to… more
    Sanofi Group (05/13/25)
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  • Master's of Medical Product Development…

    San Jose State University (San Jose, CA)
    …candidates with teaching experience in the following: industry experience in entrepreneurship, drug / medical device development, data science, regulatory ... discipline, and a minimum of 3-5 years related experience in a medical device , pharmaceutical, In Vitro Diagnostics, and/or Clinical Research Organization… more
    San Jose State University (05/06/25)
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  • Associate Director, Engineering - Medical

    Merck (Wilson, NC)
    …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 ... implementation and robust application at the site. Experience in design controls, device risk management, medical device , combination products, prefilled… more
    Merck (05/21/25)
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  • Engineer I, Medical Device Design…

    Amgen (Cambridge, MA)
    …transform the lives of patients while transforming your career. Engineer I - Medical Device Design Control Documentation Specialist **What you will do** Let's ... Quality Management - ISO 13485; Risk Management - ISO 14971; EU Medical Device requirements - Council Directive 93/42/EECStrong background in documenting… more
    Amgen (05/09/25)
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  • Medical Device Design Engineer

    ManpowerGroup (San Antonio, TX)
    Our client, a leader in the medical device industry, is seeking a Medical Device Design Engineer to join their team. As a Medical Device Design ... be part of a dynamic cross-disciplinary team supporting innovative medical device projects. The ideal candidate will...completion of waiting period consultants are eligible for:** + Medical and Prescription Drug Plans + Dental… more
    ManpowerGroup (05/17/25)
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  • Senior Quality Engineer ( Medical

    Organon & Co. (Jersey City, NJ)
    …documenting, and review of documentation to ensure compliance with applicable Medical Device Regulations and internal Organon requirements. Sr. Quality ... Engineer ( Medical Device /Combo Products) is responsible for program...and medical leave, and health benefits including medical , prescription drug , dental, and vision coverage… more
    Organon & Co. (04/26/25)
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  • GRA Device Lead

    Sanofi Group (Morristown, NJ)
    …with key stakeholders including clinical, medical affairs, Industrial Affairs ( Device Development, manufacturing, quality, supply chain) and drug product ... team is a globally diverse team supporting the medical device , combination product, digital health and...development. Combination product and drug delivery device systems technology is often exploring new territories that… more
    Sanofi Group (04/15/25)
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  • Staff Device Engineer

    Takeda Pharmaceuticals (Lexington, MA)
    …product. The Staff Device Engineer has extensive experience in medical devices for drug delivery including combination products, solid understanding ... Engineer will lead technical efforts for combination products and drug delivery device projects with limited oversight....of polymeric medical device manufacturing processes via molding and… more
    Takeda Pharmaceuticals (05/02/25)
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  • QC Associate - Medical Device

    Lilly (Indianapolis, IN)
    …requirements (eg, cGMP, 21 CFR 820, ISO 13485, ISO 194971, Canadian MDR, EU Medical Device Directive, JPAL). **Additional Preferences:** + Three or more years of ... participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical , dental, vision and prescription drug benefits; flexible benefits… more
    Lilly (05/14/25)
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