- Sanofi Group (Framingham, MA)
- …stakeholders are well-prepared and informed. + Collaborate with SMEs and Business Process Owners (BPOs) to ensure consistent and high-quality responses and support ... Global Quality functions including the quality technical experts and quality business process owners (BPOs). **Latitude of Action:** + This position reports solid… more
- Sanofi Group (Cambridge, MA)
- …processes that meet Sanofi's eco-design and economic targets and undergo successful process validation is a must. This individual may be responsible ... + Demonstrated experience leading drug substance teams through late-stage clinical and process validation (PPQ) + An ability to operate with flexibility… more
- Nitto Denko Corp. (Milford, MA)
- …and/or commercialized. This includes interfacing with clients that are nearing process performance qualification (PPQ), PAI and commercial readiness, and that are ... + Support or perform disposition of advanced oligonucleotide products for pharmaceutical use, including pharmaceutical intermediates, active pharmaceutical … more
- Amgen (Cambridge, MA)
- …The individual will be responsible for designing, conducting, and analyzing new process development, validation and requalification studies for gas sterilization ... dioxide or other gas sterilization modalities + 1+ years in gas sterilization process development, validation and routine production + 1+ years in radiation… more
- ThermoFisher Scientific (Plainville, MA)
- …and transfer that knowledge between shifts. Lead successful deployment of process improvements, quality systems and standards. **Work Hours:** Monday-Friday shift. ... deviations, Batch Lot Verification (BLV), Batch record review, change controls, validation protocols, and document changes. Organize and lead ad-hoc cross functional… more
- Bristol Myers Squibb (Devens, MA)
- …& archive completed GMP documents when required + Review work throughout the work process and at completion, in order to ensure that it has been performed properly, ... maintaining material inventory accuracy using required systems and equipment + Support process investigations & CAPAs + Provide oversight and suggestions on special… more
- Takeda Pharmaceuticals (Lexington, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... and lifecycle management. You will work within a collaborative, cross-functional Pharmaceutical Sciences team, contributing to program strategies and applying your… more
- Bristol Myers Squibb (Devens, MA)
- …detailed knowledge of total project delivery requirements from feasibility to validation , commissioning and start-up processes. + Service as point of contact ... engineering or equivalent related field. + Minimum 10 years' experience in the pharmaceutical or similar industry. + Proven experience as a master scheduler or… more
- Takeda Pharmaceuticals (Lexington, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... + Review and approve user requirements, design specifications, and verification/ validation plans + Maintain traceability between clinical needs and technical… more
- Takeda Pharmaceuticals (Boston, MA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... implement _in vitro_ screening cascades, conduct high-throughput screening and hit validation , perform SAR screenings for hit/lead optimization, and analyze hit/lead… more