• Analytical Principal Scientist (Analytical team…

    Sanofi Group (Cambridge, MA)
    …years, or a PhD with minimum of 5 years of experience in the pharmaceutical /biotech industry. A PhD in Analytical Chemistry is preferred. + Extensive experience in ... analytical method development and validation + Ability to operate independently and to prioritize...management + Having working knowledge of synthetic chemistry and pharmaceutical development + Consistent record of collaboration with scientists… more
    Sanofi Group (08/29/25)
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  • Team Lead Quality Drug Product Operations

    Sanofi Group (Framingham, MA)
    …by responding promptly to inquiries, requests and complaints + Engineering and validation tasks related to facility, utilities, and equipment + Responsible for QA ... knowledge of quality regulations and guidelines applicable to R&D pharmaceutical activities + Excellent interpersonal, communication, and facilitation skills since… more
    Sanofi Group (08/27/25)
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  • Principal Database Developer

    Cytel (Cambridge, MA)
    …systems can achieve. **Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be ... you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next...Sources + Clinical Coding + SAE Reconciliation + Data Validation and Quality Control + Blinding and Unblinding Procedures… more
    Cytel (08/14/25)
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  • Scientist I

    AbbVie (Worcester, MA)
    …Qualifications Qualifications + Bachelors degree in Biochemistry, Bioengineering, or Pharmaceutical Sciences with 5 years of relevant experience or Master's ... Degree in Biochemistry, Bioengineering, or Pharmaceutical Sciences or equivalent education with typically two years...Maurice, PA800 systems). + Experience with the qualification and validation of analytical methods in accordance with ICH, FDA,… more
    AbbVie (08/08/25)
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  • Manager, Biostatistics

    Sumitomo Pharma (Cambridge, 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 ... on SDTM/ADaM datasets and TLF specifications. + Perform programming validation for key derived datasets and oversee Quality Control...by law. Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in… more
    Sumitomo Pharma (08/02/25)
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  • Associate Director, Analytical Development…

    Takeda Pharmaceuticals (Lexington, MA)
    …and lifecycle management. You will work within a collaborative, cross-functional Pharmaceutical Sciences team, contributing to program strategies and applying your ... analytical scientists, focusing on robust and phase-appropriate method development, validation , and transfer. + Provide technical, managerial, and project… more
    Takeda Pharmaceuticals (07/02/25)
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  • Associate Director, Master Capital Project…

    Bristol Myers Squibb (Devens, MA)
    …detailed knowledge of total project delivery requirements from feasibility to validation , commissioning and start-up processes. + Service as point of contact ... engineering or equivalent related field. + Minimum 10 years' experience in the pharmaceutical or similar industry. + Proven experience as a master scheduler or… more
    Bristol Myers Squibb (06/26/25)
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  • Head of AI/ML Research

    Takeda Pharmaceuticals (Boston, MA)
    …emerging trends and technologies in AI/ML and their application to pharmaceutical research, including foundation models for protein design, diffusion-based modeling ... foundation platforms, building a continuous test-and-learn pipeline through experimental validation by collaborating across scientific disciplines and therapeutic areas… more
    Takeda Pharmaceuticals (06/15/25)
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  • Associate Director, Device Clinical Development

    Takeda Pharmaceuticals (Lexington, MA)
    …+ Review and approve user requirements, design specifications, and verification/ validation plans + Maintain traceability between clinical needs and technical ... + Minimum 5 years of combination product, medical device, or pharmaceutical industry experience + Experience with both medical devices, drug-device combination… more
    Takeda Pharmaceuticals (06/06/25)
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  • Senior Statistical Programmer

    Actalent (Boston, MA)
    …therapy programs. + Conduct regulatory submissions using R, ensuring the development, validation , and maintenance of programs for creating SDTM and ADaM datasets and ... or equivalent field. + Experience with SAS and R programming in a pharmaceutical or biotech setting. + Knowledge in CDISC, including SDTM, ADaM, metadata, controlled… more
    Actalent (09/03/25)
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