• Merck & Co. (Rahway, NJ)
    …leadership.Remain current in relevant worldwide regulatory guidance and standards. Lead /support/oversee clinical supplies production with respect to device ... applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional development teams within and external to Device more
    HireLifeScience (06/20/24)
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  • Merck & Co. (Rahway, NJ)
    …to commercialization. Our development teams ensure robust composition, primary packaging/ device , and process selection through deep fundamental understanding and ... drug products.Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within Sterile and… more
    HireLifeScience (06/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …awareness of best practices for reproducible data science, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs)- Ensure ... AI/ML deliverables- Contribute, with limited supervision, to documents submitted to regulatory or pricing authorities- Proactively identifies and manages risks in… more
    HireLifeScience (05/24/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Statistical deliverables. Contribute, with limited supervision, to documents submitted to Regulatory or Pricing Authorities. May participate as subject matter expert ... to ensure compliance with the protocol, external/internal standards, applicable regulatory guidelines, Policies, SOPs, and other relevant guidelines. Responsible,… more
    HireLifeScience (05/17/24)
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  • Device Regulatory Lead

    Sanofi Group (Bridgewater, NJ)
    **Job title: Device Regulatory Lead ( Associate Director)** + Location: Bridgewater, NJ or Swiftwater, PA or Cambridge, MA **About the job** The Global ... thought was possible. Ready to get started? **Main responsibilities** + Serve as Device Regulatory Lead on assigned project teams (early phase, late stage… more
    Sanofi Group (06/06/24)
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  • Device Development Associate

    Merck (Rahway, NJ)
    …current in relevant worldwide regulatory guidance and standards. + Lead /support/oversee clinical supplies production with respect to device component ... lead cross-functional development teams within and external to Device Development. The incumbent must be able to work... Working Group to ensure full integration of the device development activities with the clinical, regulatory ,… more
    Merck (06/20/24)
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  • Associate Director, US Advertising…

    Sanofi Group (Bridgewater, NJ)
    …the job** The Associate Director, US Advertising and Promotion serves as the regulatory lead on Review Committees (RCs). As the RC Regulatory Affairs ... **Job title: Associate Director, US Advertising and Promotion, Global Regulatory Affairs** + Location: Cambridge, MA or Bridgewater, NJ **About… more
    Sanofi Group (06/20/24)
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  • Associate Principal Scientist, Sterile…

    Merck (Rahway, NJ)
    …to commercialization. Our development teams ensure robust composition, primary packaging/ device , and process selection through deep fundamental understanding and ... products. Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within Sterile and… more
    Merck (06/28/24)
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  • SOC Analyst (IT Sr Associate 1)…

    CUNY (New York, NY)
    SOC Analyst (IT Sr Associate 1) - Provisional **GENERAL DUTIES** IT Senior Associates perform highly complex professional work in technology-related disciplines. ... They have wide latitude for independent initiative and judgment and may serve in lead roles on complex programs or projects, and/or serve as a direct supervisor of… more
    CUNY (06/25/24)
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  • Program Associate Director

    Zimmer Biomet (New York, NY)
    …respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to enable the ... key functional areas - Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio as owned by… more
    Zimmer Biomet (05/30/24)
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  • Managing Consultant - Life Sciences - Market…

    Guidehouse (New York, NY)
    …practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle today's ... all levels, to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Do you think you are up for the… more
    Guidehouse (06/15/24)
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  • Quality Manager - Kohler Ventures

    Kohler Co. (New York, NY)
    …Our mission is to build new digital businesses that empower consumers to lead healthier lives. We explore how familiar experiences can be enhanced and innovations ... a Quality Culture that will transform the company into a premier wellness device manufacturer. The ideal candidate will have demonstrated a successful track record… more
    Kohler Co. (04/13/24)
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  • Principal Field Clinical Specialist, Mitral…

    Medtronic (New York, NY)
    …Heart Business is one of the fastest growing businesses in the medical device industry and expanding rapidly to serve patients globally. The Structural Heart and ... a key role in all aspects of Intrepid TMVR/TTVR device preparation & case support + Provide technical support...specialist/clinical engineer or relevant hospital experience_ ) or + Associate degree with a minimum of 9 years of… more
    Medtronic (06/22/24)
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  • Sr Clincial Specialist Coronary Renal Denervation…

    Medtronic (New York, NY)
    …is assigned to the business unit. + Develop and maintain therapeutic and device operation knowledge; apply this knowledge to the development of well-written, clear, ... analyze literature search results + Address deficiencies and or answer questions from regulatory agencies as needed + Create and manage project schedule for each… more
    Medtronic (04/16/24)
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  • Professional and Clinical Training Manager

    Terumo Medical Corporation (Somerset, NJ)
    …part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $5+ billion in sales, 20,000+ employees worldwide and operations ... by meeting all internal and external requirements. In this role, the associate will apply project management techniques to ensure projects are completed on-time… more
    Terumo Medical Corporation (04/10/24)
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  • Senior Clinical Specialist, EndoVenous - NYC

    Medtronic (New York, NY)
    …of changes in work schedule and/or workload. + Adheres to financial, regulatory , quality compliance standards and requirements **MUST HAVE - BASIC QUALIFICATIONS:** ... YOUR RESUME_ + High School Degree and 9+ OR Associate degree and 5+ OR Bachelor's degree and 3+...knowledge of medical terminology, medical procedures and the medical device industry. + Excellent customer service skills + Excellent… more
    Medtronic (05/29/24)
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  • Managing Consultant - Life Sciences Advisory…

    Guidehouse (New York, NY)
    …practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle today's ... all levels, to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Do you think you are up for the… more
    Guidehouse (05/18/24)
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