- Sanofi Group (Cambridge, MA)
- …with a minimum of 4 years of experience in the pharmaceutical/biotech industry. A PhD in Analytical Chemistry is preferred. + Expertise in the operation of LC and ... concepts, specification setting, and cGMP, with experience in contributing to regulatory submission + Communicates effectively in individual and group settings and… more
- Bristol Myers Squibb (Cambridge, MA)
- …to address key business problems. + Communicates effectively with clinical and regulatory partners and external opinion leaders. + Builds the external reputation of ... BMS R&D via external interactions through collaborations with alliance partners, academic and government research organizations, publications and conference participation + Provides statistical consultation for ad hoc analysis requests including design of… more
- Takeda Pharmaceuticals (Boston, MA)
- …timely and accurate manner and prepares study reports for internal and regulatory use. + Scientifically assesses and recommends vendors and outsources nonclinical ... and/or fibrosis is a plus. **_EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:_** + PhD degree in Immunology, or related scientific discipline with 3+ years of… more
- Takeda Pharmaceuticals (Lexington, MA)
- …AD and cross functionally and guide junior staff. + Prepares documentation for regulatory filings, authors technical reports, may author publications. + Able to work ... on multiple programs and represent AD within PS/project teams + Complete all required training appropriate to role and function in a timely manner. **Education & Competencies (Technical and Behavioral):** + Bachelors degree with 10+ yrs relevant experience,… more
- Dana-Farber Cancer Institute (Boston, MA)
- …degree in Computer Science, Information Systems, or related field (Master's or PhD preferred). + 5 years of relevant experience in advanced analytics leveraging ... custom software applications. + Familiarity with healthcare data and regulatory environments (HIPAA, GDPR) is preferred. **KNOWLEDGE, SKILLS, AND ABILITIES… more
- AbbVie (Cambridge, MA)
- …publications of translational findings in peer reviewed journals, new drug applications and regulatory filings. Key Responsibilities: . Lead a diverse team of up to ... collaborations/partnerships in academia and industry. Qualifications Basic Qualifications: . PhD . in bioinformatics, statistics, mathematics, computer science, computational biology,… more
- Astellas Pharma (Cambridge, MA)
- …with Oncology Research overall strategy and objectives. **Qualifications:** **Required** + PhD , MD or equivalent advanced degree in a life science discipline ... area + Deep understanding of pharmaceutical product development, manufacturing, and regulatory science + Contributed to the successful transition of drug candidates… more
- Autodesk (Boston, MA)
- …team inside the Autodesk AI Lab focusing on Responsible AI **Minimum Qualifications** + PhD in Computer Science, AI/ML, or a related field with a focus on ... engineering, or manufacturing + Familiarity with AI governance frameworks and regulatory landscapes + Knowledge of fairness, accountability, transparency, and safety… more
- Takeda Pharmaceuticals (Boston, MA)
- …and process improvements. + Authors technical reports, validation documents, regulatory filings, and peer-reviewed manuscripts related to crystallization modeling ... and particle engineering methodologies. + Maintains awareness of emerging trends and tools in crystallization modeling, proactively identifies relevant vendor solutions, and actively participates in academic and industry collaborations to advance modeling… more
- UKG (Ultimate Kronos Group) (Lowell, MA)
- …Local candidates are highly preferred. **Preferred Qualifications:** + Master's degree or PhD in Computer Science or a related technical field. + Familiarity with ... area. + Understanding of internal and external business challenges and regulatory factors. Apply best practices to improve products, processes, or services.… more