- Bristol Myers Squibb (Devens, MA)
- …manufacturing operations, system enhancements and site expansion activities for Clinical manufacturing and Biologics development operations. The activities will ... under FDA regulated environment is required. + Understanding of engineering documentation such as P&IDs, Process Flow diagrams and standard operating procedures.… more
- IQVIA (Springfield, MA)
- …daily data while maintaining high standards of product support quality documentation . + Full-time commitment requiring travel locally, regionally, and nationally. + ... unleash new opportunities. \#LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- Bristol Myers Squibb (Devens, MA)
- …of S88, S95, and batch processing operations. + Expert understanding engineering documentation such as P&IDs, network diagrams, process flow diagrams, and SOPs. + ... unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency,… more
- Bristol Myers Squibb (Cambridge, MA)
- …of full-stack and ML engineers; foster better-than-best practices in code quality, documentation , and UX research. + Partner with discovery leads, IT operations, and ... unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency,… more
- Medtronic (Boston, MA)
- …processes, and systems by being accountable, having a voice and taking action. Clinical Specialists are required to be within their assigned territory each day to ... coverage as approved by regional management. To find all Cardiac Rhythm Management Clinical Specialist roles available please use #crmcs in the key word search at… more
- Medtronic (Mansfield, MA)
- …ensure project deadlines are met. + Collaborate with engineering, quality, clinical , marketing, and other departments to fulfill regulatory responsibilities. + ... Participate in internal and external audits as required. + Maintain regulatory documentation to ensure compliance. + Coordinate and prepare document packages for… more
- Medtronic (Boston, MA)
- …culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This position will sit at our Boston, MA site. ... Lead multifaceted cross-functional teams, encompassing Design, Development, Verification, Validation, Documentation . Guide them through the product development journey, ensuring… more
- Astellas Pharma (Westborough, MA)
- …range of disease indications, ranging from macular degeneration (currently in clinical trials) and other ocular indications to vascular and autoimmune disease. ... Cell Therapy Manufacturing facility in Westborough, MA as products move through clinical trials and commercialization. The Validation Manager will be a leader and… more
- ThermoFisher Scientific (Plainville, MA)
- …facial hair etc allowed, Office **Job Description** **MST Process Engineer /Scientist III, Downstream - PLA** **JOB SUMMARY/OBJECTIVE:** The primary responsibility ... and Technology activities in support of downstream technology transfer, late stage clinical , PPQ and commercial manufacturing of viral vectors. The individual will… more
- Bristol Myers Squibb (Devens, MA)
- …for handling Quality Assurance Shop Floor internal compliance and documentation tasks, routine communication to front line employees, and metrics/monitoring ... but not limited to procedures, CAPAs, change controls, impact assessments, documentation , or deviations; and represent QASF at relevant governance forums.… more
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