- Danaher Corporation (Waltham, MA)
- …clients and senior management. The essential requirements of the job include: + PhD in molecular biology, biochemistry, or related discipline with 3+ years of ... novel assays/techniques to achieve molecular biology goals + Knowledge of regulatory guidelines related analytical method development and validation + Bio-analytical… more
- Takeda Pharmaceuticals (Lexington, MA)
- …or showstoppers, verify alignment with Takeda's technology, network, business, and regulatory strategies, assess capabilities fit, ensure timeline vs. deal value ... alignment, verify process-, analytical-, formulation-development, stability data, manufacturing capacity, capabilities and supply meet the needs of the proposed program strategy and, confirm overall alignment of deal model assumptions with GMS: eg projected… more
- Sanofi Group (Framingham, MA)
- …of problems, while ensuring the highest standards of safety, environmental and regulatory compliance are maintained in the workplace. We are an innovative global ... automation techniques and applications **About You** **Basic Qualifications:** + PhD . in Computer Science, Mechanical Engineering, Robotics, Electrical Engineering,… more
- J&J Family of Companies (Cambridge, MA)
- …and external human data resources. + Partner with Clinical Development, Global Regulatory Affairs, Data Science, Patient Reported Outcomes, Statistics and other core ... with the strategies and goals of the team and enterprise. **Qualifications:** **Education** PhD with 8 years of progressive experience in a computational or physical… more
- Nanobiosym, Inc. (Cambridge, MA)
- …and build test fixtures for hardware validation and functional testing. + Support regulatory and quality processes with a focus on FDA and ISO 13485 compliance. ... + Java programming skills (preferred but not required). Preferred Qualifications: + PhD or MS/ME in EECS or related fields/experiences + LabVIEW development… more
- ThermoFisher Scientific (Boston, MA)
- …skills, and abilities to perform the job **(comparable 4+ years')** + OR PhD and previous experience that provides the knowledge, skills, and abilities to perform ... Gene and Cell therapy is desirable + Knowledge of relevant ICH and regulatory guidelines and good understanding of GMP concept + Experience with analytical support… more
- UNUM (Boston, MA)
- …services to the Benefits Center. The Medical Consultant adheres to current regulatory , claim process, and internal workflow standards as set forth in the ... other duties as assigned **Job Specifications** + Professional Degree (MD, DO, PhD , PsyD) + Active, unrestricted US medical license + Board certification required… more
- Sanofi Group (Cambridge, MA)
- …publications in peer-reviewed journals, and contributions to patent filings and regulatory submissions. Represent Sanofi at external scientific forums. + Resource ... years of immunology research experience in an academic or biopharmaceutical setting OR PhD plus minimum 10 years of immunology research experience in an academic or… more
- Fujifilm (Boston, MA)
- …and Head of site PM as required. + Compliance: Keep current on cGMP, regulatory and quality requirements that impact Company manufacturing. + All other job duties ... 10 years in the biotech or pharmaceutical environment related experience or; + M.Sc. or PhD . in Engineering or related discipline with a minimum of 10 years in the… more
- Takeda Pharmaceuticals (Lexington, MA)
- …and Global functional groups such as Medical, Publications, Medical Information, Regulatory , Statistics, and Legal. * Provide support to respective Product Medical ... and vendor management * Project management skills Preferred: * MS, PharmD, PhD , or MD degree; post-doctoral residency or fellowship * Experience managing publication… more