• Merck & Co. (Rahway, NJ)
    …advanced degree (Master's or PhD) preferred.Minimum of 10 years of experience in medical device or combination product engineering, with at least 5 years ... Job DescriptionJob Summary: -The Director of Device Technology Transfer is...technical leadership in Technology Transfer and Design Transfer for medical device and combination product component manufacturing,… more
    HireLifeScience (09/26/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …position has advanced experience working on Phase I-IV studies within the medical device and/or pharmaceutical industry across multiple therapeutic areas and ... years with Master's Degree) data management and/or related work experience in a medical device or pharmaceutical company, or similar environment (eg, CRO)… more
    HireLifeScience (09/25/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …input into development plans, study designs, and regulatory submissions. Relationships The Principal Medical Writer reports to a Director of Medical Writing. ... merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both...ready to make a difference? The Position The Principal Medical Writer is an expert in medical more
    HireLifeScience (09/26/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …the clinical development and regulatory requirements of a clinical program. Relationships The Senior Medical Writer reports to a Director of Medical Writing. ... Development Hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop… more
    HireLifeScience (09/24/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
    HireLifeScience (09/25/24)
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  • Corporate Accounts Director

    Pentax Medical (Los Angeles, CA)
    …Position Opening: DIRECTOR , CORPORATE ACCOUNTS Why JOIN Us? We are an established medical device leader that is preparing for high growth. This means that ... is to improve the standard of patient care and quality of healthcare delivery by providing the best endoscopic..., Corporate Accounts: + Advanced knowledge of the GI medical device national and corporate accounts landscape.… more
    Pentax Medical (09/12/24)
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  • Director of Connected Device

    Sanofi Group (Bridgewater, NJ)
    …will be responsible to lead the design, development, and implementation of connected medical device technologies and ensuring they meet the specific needs of ... ** Director of Connected Device Technology** **About...work experience in the area of connected & digital medical device technologies or equivalent. + Working… more
    Sanofi Group (09/14/24)
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  • Director - Device Product…

    Merck (West Point, PA)
    …technical support and product stewardship for several key products in our company's medical device and combination products portfolio. This role will ensure the ... **Job Description** **Job Summary:** The Director of Device Product Stewardship will...stewardship across assigned products, including managing ongoing changes to medical device and combination product designs and… more
    Merck (09/26/24)
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  • Director , Device Technology…

    Merck (Rahway, NJ)
    …advanced degree (Master's or PhD) preferred. + Minimum of 10 years of experience in medical device or combination product engineering, with at least 5 years in a ... **Job Description** **Job Summary:** The Director of Device Technology Transfer is...technical leadership in Technology Transfer and Design Transfer for medical device and combination product component manufacturing,… more
    Merck (09/26/24)
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  • Senior Director and Regulatory Platform…

    Takeda Pharmaceuticals (Cambridge, MA)
    …and meetings with global health authorities + Reviews and approves medical device development design control documentation, including technology transfer ... a device and/or combination product role in pharmaceuticals and/or medical devices industry including experience in regulatory CMC; international experience is a… more
    Takeda Pharmaceuticals (09/24/24)
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  • Senior Specialist, Medical Device

    Merck (Wilson, NC)
    …products. + Experience with injection molding and working with medical device suppliers. + Experience leading Quality Management System gap assessments ... MDCP Operations Lead position will serve as the primary medical device and combination product (MDCP) point...liaison between the site and global MDCP teams (Technical, Quality , etc.), providing hands-on shop floor perspective and advocating… more
    Merck (09/21/24)
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  • Cardiac Implantable Electronic Device

    Dartmouth Health (Lebanon, NH)
    …* f) Assist in managing device recalls/advisories. * g) Assist the DHDC Medical Director in education, quality and safety control, and quality ... operations of the DHDC and works closely with the Medical Director of the device ...j) Collect survey responses from patients to include in quality and safety improvement measures. * k) Assist the… more
    Dartmouth Health (10/02/24)
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  • Lead, Plasma-Derived Therapies - Global Regulatory…

    Takeda Pharmaceuticals (Cambridge, MA)
    …engineering discipline (advanced degree preferred) + 8+ years of biotechnology, pharmaceutical or medical device industry experience + 5+ years of regulatory ... therapies to patients worldwide. Join Takeda as an Associate Director , Global Reg Affairs Device , PDT in...the development, registration, commercialization and lifecycle management of the medical , ancillary, or combination device in the… more
    Takeda Pharmaceuticals (09/25/24)
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  • Regulatory - Medical Device Engineer

    Actalent (Schoolcraft, MI)
    …company strategy and Quality Management System (QMS) for an evolving medical device company. The role includes managing product regulatory strategy, ... Quality Engineer The Regulatory Affairs Manager is a...experience with regulatory affairs/regulatory compliance + Experience within the medical device or pharmaceutical industry (preferably 3+… more
    Actalent (09/28/24)
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  • RN Ventricular Assist Device (VAD) Clinical…

    HonorHealth (Scottsdale, AZ)
    …collaboration. The VAD Clinical Program Manager will work closely with the Network Director and Medical Directors to develop strategy. The CPM will coordinate ... more. HonorHealth is looking for an RN Ventricular Assist Device (VAD) Clinical Manager to support our new, inviting...Reporting/Data Management: The CAD CPM supports CVSL Pillar Chiefs, Medical Directors, and Quality Consultants in … more
    HonorHealth (08/28/24)
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  • Director Of Quality

    Globus Medical, Inc. (Limerick, PA)
    …regulatory compliance with US FDA, State, OSHA and international medical device regulations and ISO 13485 quality system requirements. Responsible for ... and finishing operations associated with orthopedic implants and related medical devices. The Director of Quality...US FDA, State, OSHA, and international medical device regulations based on ISO 13485 quality more
    Globus Medical, Inc. (09/28/24)
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  • Director , Quality - Service…

    ICU Medical (Salt Lake City, UT)
    …This ensures consistent and high- quality investigations, servicing, and repair of medical devices on a global scale. The Director collaborates closely with ... *Position Summary* The Director , Quality plays a vital role...investigation of global complaints related to consumables and serialized medical devices. This position is accountable for ensuring that… more
    ICU Medical (09/12/24)
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  • National Director , Field Medical

    Inovio Pharmaceuticals (Plymouth Meeting, PA)
    …and overall direction to the Medical Science Liaison (MSL) and Clinical Device Liaison (CDL) teams. The National Director , Field Medical Affairs ... and cancers. For more information, visit www.inovio.com . Job summary The National Director , Field Medical Affairs (FMA) will be responsible for providing… more
    Inovio Pharmaceuticals (07/24/24)
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  • Director , Service & Repair…

    Integra LifeSciences (Cincinnati, OH)
    …with corporate policies, US Food and Drug Administration regulations, ISO 13485, the Canadian Medical Device Regulations (CMDR), the EU Medical Device ... making headway to help improve outcomes. **SUMMARY DESCRIPTION** The Director , Service & Repair and Quality Distribution...discipline required with min 15 years' experience in the medical device or pharmaceutical industry and minimum… more
    Integra LifeSciences (09/30/24)
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  • Director , Systems Engineering

    ZOLL Medical Corporation (Chelmsford, MA)
    …domain and staying current on the latest technologies and trends in the medical device industry. Knowledge, Skills and Abilities + Proven leadership and ... devices. + Working knowledge and experience with electromechanical software-controlled medical device systems, such as microprocessor systems design, low-level… more
    ZOLL Medical Corporation (08/01/24)
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