• Global Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    **Job title** : Global Regulatory Affairs Device Lead (Associate Director) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the ... could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the… more
    Sanofi Group (10/23/25)
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  • Global Regulatory Affairs CMC…

    Sanofi Group (Morristown, NJ)
    …we chase the miracles of science to improve people's lives. The Global Regulatory Affairs (GRA) CMC & Device Organization within Sanofi R&D serves ... **Job Title:** Global Regulatory Affairs CMC...**Job Title:** Global Regulatory Affairs CMC lead **Location:** Framingham,...GRA CMC Lead within our GRA CMC & GRA Device Organization, you'll drive global regulatory more
    Sanofi Group (10/15/25)
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  • GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting ... pathways. The team is accountable for developing and implementing global regulatory strategies for device ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (09/20/25)
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  • Senior Manager, Regulatory Affairs

    Stryker (Mahwah, NJ)
    …launches and patient-specific solutions. You will work across the Regulatory Affairs teams and cross-functional partners with global locations, time zones ... **Senior Manager, Regulatory Affairs - Joint Replacement Division**...provide leadership and coordination of the Joint Replacement divisions' global regulatory strategies, submission preparation and approvals… more
    Stryker (12/04/25)
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  • Senior Regulatory Affairs Specialist

    Pentax Medical (Montvale, NJ)
    …devices and solutions to the global medical community. Position Opening: Senior Regulatory Affairs Specialist Why JOIN Us? We are an established medical ... for Endoscopes and Speech, Voice and Swallowing devices, meet global regulatory standards. This role will collaborate...shaping the future of medical technology. Responsibilities of Senior Regulatory Affairs Specialist : + Coordinate with… more
    Pentax Medical (10/24/25)
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  • Medical Devices, Regulatory Affairs

    Meta (New York, NY)
    …discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. Experience working ... **Summary:** We're seeking a regulatory affairs specialist to join our...to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals.You… more
    Meta (10/08/25)
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  • Director, US Regulatory Affairs

    Sanofi Group (Morristown, NJ)
    …other relevant discipline + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs , with 5+ years specifically within advertising ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion...training and team leadership opportunities. We are an innovative global healthcare company with one purpose: to chase the… more
    Sanofi Group (10/23/25)
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  • Global Medical Affairs Director…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA / Morristown, NJ **About the job** **About us:** In order to pursue ... engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs ...unmet needs. Sanofi is recruiting a new Director in Global Medical Affairs (GMA) based in Cambridge,… more
    Sanofi Group (10/02/25)
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  • Director, SM Medical Affairs , Specimen…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …Description** We are **the makers of possible** ! BD is one of the largest global medical technology companies in the world. _Advancing the world of health_ (TM) is ... possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve....directly to the business unit Vice President of Medical Affairs , the Director of Medical Affairs has… more
    BD (Becton, Dickinson and Company) (09/20/25)
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  • Medical Affairs Manager IPD

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …the core team, aiding product development, remediation projects, and meeting medical device regulatory needs. + Review, comprehend, and compose performance and ... role in crafting the future of medical technology and making a tangible impact on global health. **Responsibilities:** + Present the medical affairs role within… more
    BD (Becton, Dickinson and Company) (10/26/25)
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  • Manager, Medical Affairs Strategy

    IQVIA (New York, NY)
    **Manager, Medical Affairs Strategy** **Overview** IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services ... of innovative medical treatments. Our diverse client base includes the global top 20 pharmaceutical, medical device , and biotechnology companies… more
    IQVIA (11/04/25)
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  • Director of Scientific Affairs , COP

    Colgate-Palmolive (New York, NY)
    …York, New York, United States **Who We Are** Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral ... that address a wide range of oral health needs. The Director of Scientific Affairs for Colgate Oral Pharmaceuticals is a pivotal role responsible for leading and… more
    Colgate-Palmolive (10/15/25)
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  • Global Labeling Lead Specialist

    Kelly Services (Bridgewater, NJ)
    …obtaining regulatory approvals + Knowledge of pharmaceutical, consumer or medical device industry regulatory affairs discipline throughout the product ... ** Regulatory Affairs Specialist Labeling** Kelly(R) Science...SKILLS** + Knowledge of pharmaceutical, consumer or medical device industry product labeling processes for review and… more
    Kelly Services (11/24/25)
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  • Senior RA Specialist

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …510(k), Q-Sub), EU technical documentation under MDR, and other global regulatory filings. + Evaluate medical device regulations and lead the development ... **Job Description Summary** The Senior Regulatory Affairs (RA) Specialist will represent...change control, ensuring compliance with US, EU, and other global regulatory requirements. + Author FDA submissions… more
    BD (Becton, Dickinson and Company) (11/14/25)
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  • Principal SaMD Technical Program Manager

    Wolters Kluwer (New York, NY)
    …enabling engineering teams to operate at high velocity while ensuring strict compliance with global regulatory standards such as FDA, EU MDR, ISO 13485, and IEC ... The Principal SaMD TPM acts as a bridge between engineering, product, regulatory affairs , clinical, and quality assurance teams, facilitating strategic… more
    Wolters Kluwer (12/04/25)
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  • Digital Medical Engagement Director

    Pfizer (New York, NY)
    …Identify innovative digital and social media solutions that align to the impact the Global Medical Affairs strategy and shape the digital roadmap and quickly ... and relevance. **Cross-functional Collaboration around Medical Governance** + Liaise with Global and US internal stakeholders, including Medical, Regulatory ,… more
    Pfizer (12/12/25)
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  • Sr. Manager, Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …by closely working with MTP internal colleagues in various functions (Quality Assurance, Regulatory Affairs , Marketing, Market Access, Medical Affairs , Drug ... effectively with colleagues in Supply Chain, Accounting, Market Access, Quality Assurance, Regulatory Affairs , Finance, etc. of Tanabe Pharma Group, including… more
    Mitsubishi Chemical Group (09/24/25)
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  • Executive Director - Non-Clinical Safety…

    Organon & Co. (Jersey City, NJ)
    …cross-functional interactions with early clinical development, late-clinical development, regulatory affairs , safety and pharmacovigilance, Chemistry, ... Manufacturing and Controls (CMC), medical affairs and business development are critical to the success...to inform mitigation strategies in accordance with regional and/or global regulatory requirements. + Actively participate in… more
    Organon & Co. (11/18/25)
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  • Senior Director, Portfolio Management, Oncology

    Danaher Corporation (New York, NY)
    …collaborating with cross-functional teams including Product Management, Legal, IP, Finance, R&D, Regulatory Affairs , Clinical Affairs , Sales & Marketing, ... of people worldwide - and we're using our unmatched global scale and proven playbook to make it happen,...to execute with supporting organizations (sales, commercial marketing, medical affairs , R&D, manufacturing, regulatory , quality, etc.) on… more
    Danaher Corporation (12/12/25)
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  • Technical Writer II

    Adecco US, Inc. (Morristown, NJ)
    …organizational templates. + Collaborate with cross-functional teams including Quality, Manufacturing, Global Regulatory Affairs , and Contract Manufacturing ... variations, and annual reports. + Prepare and evaluate change controls for global regulatory impact; occasionally author technical reports, position papers,… more
    Adecco US, Inc. (12/11/25)
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