• Regulatory Affairs Associate

    Englewood Lab, Inc (Totowa, NJ)
    Title: Regulatory Affairs Associate Reports to: Manager of Regulatory Affairs Department: Quality / Regulatory Responsibilities: + Assist the ... of the Head of Quality / Regulatory . + Assist the Manager of Regulatory Affairs during periodic quality reviews, regulatory updates, and annual GMP… more
    Englewood Lab, Inc (12/11/24)
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  • Regulatory Affairs Associate

    ManpowerGroup (Clark, NJ)
    **Senior Regulatory Affairs Associate (Multiple position)** **133 Terminal Ave. Clark, NJ - Onsite role** **6+ month contract with high potential for ... to join their innovative team. Are you a **Senior Regulatory Affairs Associate ** with a...to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup… more
    ManpowerGroup (01/03/25)
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  • Associate Principal Scientist,…

    ManpowerGroup (Rahway, NJ)
    JOB TITLE / VERSION: Associate Principal Scientist, Regulatory Affairs DIVISION- R&D DEPARTMENT: Global Regulatory Affairs - CMC LOCATION: Rahway, NJ ... Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in… more
    ManpowerGroup (01/03/25)
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  • Associate Principal Scientist,…

    System One (Rahway, NJ)
    Job Title: Associate Principal Scientist, Regulatory Affairs Location: Rahway, NJ (Hybrid) Hours/Schedule: Mon- Fri; 8am- 5pm Type: Contract Responsibilities ... Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in… more
    System One (01/01/25)
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  • Associate Director, Regulatory

    Bristol Myers Squibb (Madison, NJ)
    …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
    Bristol Myers Squibb (01/03/25)
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  • Associate Director, US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …More Years in the pharmaceutical industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA filing to FDA preferred ... support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review… more
    Daiichi Sankyo Inc. (12/18/24)
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  • Associate Director, Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …pharmaceutical industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Associate Director, US Medical…

    Bristol Myers Squibb (Madison, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, US Medical, Multiple Myeloma will report to the Director, US ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will support the… more
    Bristol Myers Squibb (01/02/25)
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  • Senior Regulatory & Compliance Specialist

    Catalent Pharma Solutions (Somerset, NJ)
    …NJ is hiring a Senior Regulatory and Compliance Specialist for the Regulatory Affairs Group. The Senior Regulatory and Compliance Specialist candidate ... and the greater organization as it touches various functional areas including: Supplier Quality , Regulatory Compliance, DEA, and Quality Management Systems.… more
    Catalent Pharma Solutions (12/27/24)
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  • Regulatory Planning Manager (Hybrid)

    RWJBarnabas Health (Somerset, NJ)
    …should be in a closely related field such as health/business administration, regulatory compliance, accreditation or licensure associate , business development or ... Regulatory Planning Manager (Hybrid) - Somerset, NJReq #:0000170498.../ Management Status:Full-Time Shift:Day Facility:RWJBarnabas Health Corporate Services Department:External Affairs and Policy Location: SBC Corporation, Somerset, Somerset, NJ… more
    RWJBarnabas Health (10/18/24)
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  • Health Care Regulatory Counsel (Hybrid)

    VNS Health (Manhattan, NY)
    …as necessary and appropriate. + Collaborates with cross-functional teams, including Operations, Quality , IT, Compliance, Government Affairs , and Risk, to ensure ... compliance and identify risk areas. Serves as the primary liaison to outside regulatory counsel. Works within the Chief Legal and Risk Officer Organization ("CLRO")… more
    VNS Health (12/13/24)
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  • Legal Associate

    City of New York (New York, NY)
    …researcher, a clear and concise writer, a creative thinker, and a team player. The Associate 's work product must be of high quality , timely and well organized, ... Only candidates under consideration will be contacted. The Legal Associate (" Associate ") will report directly to, and...General Counsel and become an expert in the City's regulatory process and other legal issues that impact the… more
    City of New York (11/07/24)
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  • Associate Director, Technical Lead, Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    Affairs , Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory /Risk Management, Quality Assurance, Medical Affairs , ... design efficient, adaptable, and scalable architectures in accordance with company policies, regulatory standards, and integration methodology. 15 E - Work with the… more
    Daiichi Sankyo Inc. (12/13/24)
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  • Associate Principal Scientist, General…

    Merck (Rahway, NJ)
    …Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs , and Global Regulatory Affairs and Clinical Safety ... **Job Description** The Associate Principal Scientist, General Medicine Publications Medical Writing, works with scientists in our company's Research Labs and… more
    Merck (12/24/24)
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  • Associate Director, Global Oncology…

    Sanofi Group (Bridgewater, NJ)
    **Job title** : Associate Director, Global Oncology Corporate Communications **Location:** Cambridge, MA 50% remote working; limited travel expected. **About the ... of patients around the world. Sanofi is looking for a proactive, high-energy Associate Director to join the Global Specialty Care Communications team to support… more
    Sanofi Group (12/19/24)
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  • Associate General Counsel for Real Estate…

    City of New York (New York, NY)
    …municipal housing preservation and development agency. Its mission is to promote quality housing and diverse, thriving neighborhoods for New Yorkers through loan and ... of the affordability of the existing housing stock, enforcement of housing quality standards, and educational programs for tenants and building owners. Your team:… more
    City of New York (11/22/24)
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  • Associate Director - Health Outcomes…

    Lilly (New York, NY)
    …Pharmacoeconomics/health outcomes, formulary management, technology assessment/value frameworks, quality measures, health policy expertise along with the ... + Stay abreast of emerging science, environmental trends, healthcare policy, and regulatory actions relevant to US population-based decision-makers + Serve as a… more
    Lilly (12/07/24)
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  • Associate Director, Consumer Marketing - US…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Associate Director, Consumer Marketing - US Rare Hematology **Location** : Cambridge, MA **_About the Job_** This role will drive consumer marketing ... include, HCP marketing, Global Marketing, Sales, Research & Development, Medical Affairs , Business Development, Market Research, Life Cycle Management and Finance… more
    Sanofi Group (12/03/24)
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  • Distinguished Scientist, Product Development Team…

    Merck (Rahway, NJ)
    …with a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We… more
    Merck (12/19/24)
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  • Clinical Research Coordinator

    Hackensack Meridian Health (Edison, NJ)
    …compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries ... as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within… more
    Hackensack Meridian Health (12/06/24)
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