• Research Analyst 1- Immunology

    Charles River Laboratories (Shrewsbury, MA)
    …+ Analyze basic to moderately complex laboratory assays based on protocols and in compliance with SOPs and GLP regulations. + Record project data in accordance with ... Zero to two years related laboratory experience, preferably in a pharmaceutical or contract laboratory environment. An equivalent combination of education and… more
    Charles River Laboratories (08/28/25)
    - Related Jobs
  • Operating Engineer - (1st or 2nd Class Engineer…

    Mentor Technical Group (Boston, MA)
    …and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy ... Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering… more
    Mentor Technical Group (08/27/25)
    - Related Jobs
  • Instrumentation/Calibration Technician

    Mentor Technical Group (Boston, MA)
    …and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy ... Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering… more
    Mentor Technical Group (08/27/25)
    - Related Jobs
  • Oncology Regional Medical Scientific Associate…

    Merck (Boston, MA)
    …management, communication, and networking skills + A thorough comprehension of FDA , OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant ... to the pharmaceutical industry and its customers + Ability to organize,...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los… more
    Merck (08/23/25)
    - Related Jobs
  • Sr. Director, Product Development

    J&J Family of Companies (Danvers, MA)
    …development lifecycle. + Drive the successful launch of new products, ensuring compliance with all regulatory requirements and industry standards. + Drive adoption ... or related field required + Strong knowledge of medical device regulations ( FDA , MDR, etc.) required + Experience launching a complex electromechanical platform… more
    J&J Family of Companies (08/16/25)
    - Related Jobs
  • Principal Scientist / Principal Engineer - Peptide…

    Cambrex High Point (Waltham, MA)
    …the transformation of research, development, and manufacturing across the pharmaceutical and fine chemical industries where organic chemistry underpins product ... QA, QC, regulatory, and supply chain to ensure technical alignment and compliance . + Troubleshoot scale-up issues, support deviation investigations, and lead process… more
    Cambrex High Point (08/08/25)
    - Related Jobs
  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …This role is responsible for ensuring the robustness, scalability, and compliance of downstream operations through effective technology transfer, validation support, ... operations. + Experience with cGMP manufacturing environments and regulatory requirements ( FDA , EMA, ICH). + Familiarity with process validation principles and CPV.… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
    - Related Jobs
  • Translational Sciences Lead - Immunology

    Takeda Pharmaceuticals (Boston, MA)
    …employee works closely with other members of the NTS team and with Pharmaceutical Sciences team to generate preclinical data package for regulatory filings (IND) and ... programs. + Independent execution and interpretation of experiments in compliance with appropriate global regulatory guidance. + Effective and independent… more
    Takeda Pharmaceuticals (07/12/25)
    - Related Jobs
  • Associate Director, Global Regulatory Affairs, CMC…

    Takeda Pharmaceuticals (Boston, MA)
    …of global cross-functional teams which require experienced interpretation of applicable EMA/ FDA /ICH/WHO/Global regulations to ensure CMC compliance within the ... registration strategies. You will be RA CMC member on Regulatory, Pharmaceutical Development, and Production project teams throughout clinical development and… more
    Takeda Pharmaceuticals (07/08/25)
    - Related Jobs
  • Vice President, Health Digital/Social Strategy

    FleishmanHillard (Boston, MA)
    …Journalism, or a related field; Master's a plus. + Working knowledge of healthcare compliance requirements (eg, FDA , HIPAA, OPDP). + Strong grasp of digital ... web, paid media, and AI-powered communications for health and pharmaceutical clients. + Develop integrated, multi-stakeholder campaigns targeting healthcare… more
    FleishmanHillard (07/01/25)
    - Related Jobs