- System One (Andover, MA)
- Job Title: Associate Scientist Location: Andover, MA Work schedule: Mon- Fri, 1st shift Type: Contract Overview The Associate Scientist will be a part of ... equipment and associated documentation. Requirements + Bachelor's Degree or Associate Degree in a relevant discipline (Chemical engineering, Bioprocessing,… more
- Takeda Pharmaceuticals (Boston, MA)
- …you and empower you to shine? Join us as a PV Risk Management Scientist / Associate Director. At Takeda, we are transforming the pharmaceutical industry through ... strive for excellence in everything we do. As an Associate Director/ PV Risk Management Scientist , being...with partner global functions (eg Clinical Science, Med Affairs, Regulatory Affairs, Biostats) to ensure alignment of global position… more
- Bristol Myers Squibb (Cambridge, MA)
- …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... teams. + Direct and support publications in high quality scientific, technical or medical journals. **Qualifications** : + PhD degree in a relevant field (eg… more
- Kelly Services (Boston, MA)
- Kelly Science is seeking an Associate Scientist for a cell and gene therapy focused client located in the Boston, MA area. Salary: $70,000-90,000/year Job Duties ... with analytical method qualification, transfer, validation and general understanding of regulatory requirements for biotherapeutics development is a plus. As part of… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …application is true to the best of my knowledge. **Job Description** As an Associate Scientist working in the Analytical Development Early Development team, you ... work streams + Authoring of technical reports and contributes to regulatory filings **Education and Experience:** **Required:** + Bachelors degree in Pharmaceutics,… more
- Bristol Myers Squibb (Boston, MA)
- …with disease and lab scientists, as well as BMS members from clinical, medical , commercial, regulatory , and diagnostics. Individual will also engage with ... of this role are to act as a lead scientist to implement and deliver on biomarker strategies for...data generated to support asset development and contribute to regulatory submissions. This individual will work on cross-functional project… more
- Dana-Farber Cancer Institute (Methuen, MA)
- …including bone marrow smears processing. + Perform other duties as assigned. + Associate Degree in Medical Laboratory Technology or equivalent (ie, Military ... or National Credentialing Agency (NCA) or equivalent agency as a Medical Technologist, Clinical Laboratory Scientist , or specialty certification. **KNOWLEDGE,… more
- Amgen (Cambridge, MA)
- …various global manufacturing sites. This role requires a deep understanding of medical device design, manufacturing processes, and regulatory requirements. Key ... Qualifications:** + 6-8 years of progressive experience as an engineer or scientist in relevant fields ( medical device development, manufacturing, etc.) +… more
- Sanofi Group (Cambridge, MA)
- …expertise with the COA team; provide direction and delegate specific tasks to associate COA scientist + Implement new methodologies and promote innovative ... new COA instruments; the development of briefing books or dossiers for regulatory consideration of COAs Internal customers include primarily Research and Development… more
- Merck (Boston, MA)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more