• Head of Immunology Clinical Development

    Sanofi Group (Cambridge, MA)
    …larger teams. + Significant regulatory experience, with preference for experience with global regulatory submissions. + This position may require up to 25% ... could be critical in helping our teams accelerate progress. We are an innovative global healthcare company with one purpose: to chase the miracles of science to… more
    Sanofi Group (10/13/25)
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  • Senior Manager Cleaning Validation

    Bristol Myers Squibb (Devens, MA)
    …cleaning validation. + Maintain up-to-date knowledge of industry best practices and regulatory expectations for cleaning validation. + Lead and support projects ... and management of the cleaning validation program, ensuring alignment with regulatory requirements and industry best practices. + Develop, write, and execute… more
    Bristol Myers Squibb (11/06/25)
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  • Data Center Energy Strategist

    Iron Mountain (Boston, MA)
    …Iron Mountain is seeking a dynamic Data Center Energy Strategist to join our Global Data Centers team. In this role, you will be responsible for developing, ... data center sites. You will partner across business, engineering, utility, regulatory , and sustainability teams to ensure reliable, cost-effective, and resilient… more
    Iron Mountain (11/03/25)
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  • Quality Systems Engineer- Self Inspection…

    Astellas Pharma (Westborough, MA)
    …ensure continuous compliance with current Good Manufacturing Practices (cGMP), company policies, and global regulatory standards. This role plays a vital part in ... of stem cell and regenerative medicine therapies. Astellas is an R&D-driven global pharmaceutical company whose philosophy is to contribute to the improvement of… more
    Astellas Pharma (11/24/25)
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  • Manager, PVRM

    Sumitomo Pharma (Boston, MA)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties… more
    Sumitomo Pharma (10/30/25)
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  • Head of US Reimbursement and Public Policy

    Sanofi Group (Cambridge, MA)
    …and key stakeholders to advance Sanofi's policy objectives. We are an innovative global healthcare company, committed to transforming the lives of people with immune ... the world. **Main Responsibilities** **Policy Strategy & Leadership** + Define and lead Sanofi's US reimbursement and public policy strategy, aligned with business… more
    Sanofi Group (10/04/25)
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  • Sr. Director, Design and Supplier Quality

    Candela Corporation (Marlborough, MA)
    …/ regulatory / compliance. . Working understanding of relevant global /regional medical device regulations and standards with particular emphasis on MDSAP, MDR, ... State/Territory **Massachusetts** **Company Overview:** Candela Corporation is a leading global aesthetic device company with a comprehensive product portfolio and… more
    Candela Corporation (09/30/25)
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  • Senior Water Conveyance Project Manager

    AECOM (Boston, MA)
    …to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and ... positive and tangible impact around the world. We're one global team driven by our common purpose to deliver...Responsibilities may include but not limited to: + Technical lead for pipeline rehabilitation and design. + Interface with… more
    AECOM (11/12/25)
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  • Director

    Pfizer (Cambridge, MA)
    …AI, and data-driven insights. We are seeking a Program Manager to lead the vision, strategy, and roadmap for foundational platform services, infrastructure hosting, ... to deliver secure, scalable, and compliant platform solutions that support global R&D efforts. **Key Responsibilities** **Leadership & Strategy** + Build and… more
    Pfizer (11/24/25)
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  • Sr Manager, Quality Assurance

    Hologic (Marlborough, MA)
    …You'll partner cross-functionally, mentor a high-performing team, and ensure adherence to global regulatory standards. If you're ready to make a meaningful ... we are seeking a **Senior Manager, Quality Assurance** to lead the development, implementation, and maintenance of our divisional...Part 820, ISO 13485:2016, EU MDR 2017/745, and other global regulatory standards. + Expertise in managing… more
    Hologic (11/14/25)
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