• Postdoctoral Fellow - DNA Origami

    Harvard University (Cambridge, MA)
    …+ Maintain a high level of expertise through continuous engagement with scientific literature. Additional Information: + We encourage candidates to apply by August ... goals. + Full list of publications, and copies of up to three relevant scientific papers. + Names and contact information of three references (expected to provide… more
    Harvard University (08/02/25)
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  • Executive Medical Director, Oncology Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …from ongoing internal and external studies, assessing the medical and scientific implications and making recommendations that impact regional and global development ... external compounds (alliances and in-licensing opportunities) + Primary interface with Medical Affairs team for strategy and to support of product commercial efforts… more
    Takeda Pharmaceuticals (07/28/25)
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  • Senior Manager - Biointerfaces and Regenerative…

    ConvaTec (Lexington, MA)
    …including Applied Research, New Product Development, Marketing, Medical and Clinical Affairs , Market Access, and External Innovation, to develop technologies that ... contributing to Convatec's reputation as a leader in innovation and scientific excellence. **Key Responsibilities:** **Lead and Manage the Biointerfaces and… more
    ConvaTec (07/22/25)
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  • Senior Product Manager, Global Product Management

    Cole-Parmer (Franklin, MA)
    …development in collaboration with Research & Development, Operations, Regulatory Affairs and Commercial teams. Implement appropriate programs to either internally ... support both the internal MolDx sales team and global distribution channels. + Scientific marketing for the assigned portfolio and markets, including the creation of… more
    Cole-Parmer (07/19/25)
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  • Clinical Documentation Global Head

    Sanofi Group (Cambridge, MA)
    …teams **Formal Education And/Or Experience Required:** + PhD/Master degree in scientific discipline, PharmD, or medically qualified with: + Min 15 years ... of experience working in clinical development and/or regulatory affairs + Min 10 years of leading an internationally dispersed organization managing budgets,… more
    Sanofi Group (07/02/25)
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  • Global Therapeutic Area Head, Dermatology,…

    Sanofi Group (Cambridge, MA)
    …as alliances, analysts and the investment community, patient organizations, and scientific institutions is required) + Demonstrated ability to **work collaboratively ... including marketing brand teams, market research, market access, medical affairs , business development, regulatory, research & development, manufacturing, finance… more
    Sanofi Group (06/12/25)
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  • Senior Specialist, Drug/Device Combination…

    Merck (Boston, MA)
    …device, complex combination product kits, prefilled syringes, autoinjectors, and related scientific /technical concepts and techniques are a must for this position. ... External Manufacturing, R&D, Quality, Operations, Product Development groups, Regulatory Affairs , Procurement, and suppliers. **Key Functions** Work Independently and… more
    Merck (08/29/25)
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  • Emergency Response Section Chief-Environmental…

    State of Massachusetts (Worcester, MA)
    *Who We Are:* The Executive Office of Energy and Environmental Affairs (EEA) seeks to protect, preserve, and enhance Massachusetts' environmental resources and ... officials. * Experience working in personal protective equipment (PPE) and scientific assessment and monitoring equipment. * Experience in investigating and… more
    State of Massachusetts (08/28/25)
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  • Lead, Contamination Control & Sterility Assurance

    Sanofi Group (Framingham, MA)
    …(Development, Manufacturing, Engineering, Digital, Quality, Procurement, and Regulatory Affairs ) + Demonstrated project management experience in complex, ... With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us… more
    Sanofi Group (08/27/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    affairs , quality assurance, and other departments to drive scientific excellence, resolve complex technical issues, and ensure compliance with applicable ... regulations and guidelines. + Provide CMC functional representation on wider cross-functional program development teams, ensuring all CMC considerations are accounted for in wider clinical development plans. + Serve as early-stage CMC representative of the… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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