- Sanofi Group (Cambridge, MA)
- **Job Title:** Clinical Outcome Assessment (COA) Lead **Grade:** L3 **Hiring Manager :** Benoit Arnould **Location** : Cambridge, MA or Morristown, NJ (Hybrid policy ... other methods. The COA team is part of Sanofi's Global Research and Development (R&D), and reports into the...COA team include the development of a disease conceptual model ; the selection of COA instruments to measure specific… more
- Bristol Myers Squibb (Devens, MA)
- …operating model . + Builds and continuously develops a high-performing global Quality team. + Fosters a culture of accountability, integrity, collaboration, and ... their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** This global executive role shapes and drives the Corporate Quality vision,… more
- Bristol Myers Squibb (Devens, MA)
- …up to operator interfaces and databases. + Work in collaboration with Validation , Quality and Manufacturing Engineering and Manufacturing operations to keep the ... on OSI PI data historian applications is preferable. + Experience on automation validation (DeltaV, MES, PI) in GMP environment that includes test script generation… more
- Bristol Myers Squibb (Devens, MA)
- …improve operational robustness and efficiency. + Work in collaboration with Validation , Quality and Manufacturing Engineering and Manufacturing operations to keep ... environment required, preferably in chemical or biotechnology. * Experience with Validation Lifecycle Management Systems ( Valgenesis , or similar). * Experience… more
- Bristol Myers Squibb (Devens, MA)
- …is seeking an Associate Director, Principal Product Quality Leader (PQL), in Global Product Quality to support commercial projects within the Cell Therapy ... for a commercial program along with associated regulatory expectations and global compliance requirements. T he individual will provide technical expertise and… more
- Bristol Myers Squibb (Cambridge, MA)
- …with deep expertise in assay and IVD development-including analytical validation , clinical development, manufacturing, and global regulatory submissions ... Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for biomarkers and diagnostics, focusing on early-stage… more
- Bristol Myers Squibb (Devens, MA)
- …defining and driving strategic Quality Control (QC) Excellence programs across BMS's global cell therapy network. This role will be responsible for driving alignment ... Develop, implement, and continuously improve the QC Excellence strategy for global QC sites, focusing on method harmonization, performance optimization, and… more
- Bristol Myers Squibb (Cambridge, MA)
- …a focus on cancer immunology and next-generation biotherapeutic target identification, validation , mechanism of action and optimization studies. This position is ... and 3D cell culture and manipulation of complex cellular model systems (organoid, immune and stromal cell co-culture, and...+ US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to… more
- Bristol Myers Squibb (Devens, MA)
- …their work. + Completes documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. + Solves ... specifications) by performing area disinfection regiment as required to meet global Health Authority requirements. **Knowledge and Skills:** + Knowledge of cGMP… more
- Bristol Myers Squibb (Devens, MA)
- …records. + Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. + Performing ... specifications) by performing area disinfection regiment as required to meet global Health Authority requirements. **Knowledge and Skills:** + Driven and motivated… more