- Charles River Laboratories (Boston, MA)
- …by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment. ... worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your… more
- NTT DATA North America (Canton, MA)
- …practices, governance frameworks, and compliance standards. Ensure alignment with GxP, FDA , EMA, and other regulatory requirements throughout project delivery + ... + Proven success in delivering SAP solutions in regulated environments (eg, GMP , GxP) + Deep understanding of Life Sciences business processes and compliance… more
- Bristol Myers Squibb (Devens, MA)
- …tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. + Qualifies new employees on assigned curriculum required of their job ... to resolve. **Knowledge and Skills:** + Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing preferred. + Must… more
- Medtronic (Danvers, MA)
- …+ Problem-solving skills and a knack for troubleshooting. + Experience with GMP requirements and industry requirements for FDA regulated industries such ... as medical devices or pharmaceutical manufacturing + Experience in extrusion processes is a plus. Please note that we are unable to sponsor work visas or provide relocation assistance for this position. Only candidates who are currently authorized to work in… more
- Charles River Laboratories (Cambridge, MA)
- …by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment. ... worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your… more
- Charles River Laboratories (Cambridge, MA)
- …by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment. ... proudly supported the development of 86% of the drugs approved by the FDA in 2021. **Equal Employment Opportunity** Charles River Laboratories is an Equal… more
- Charles River Laboratories (Cambridge, MA)
- …by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment. ... worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your… more
- Bristol Myers Squibb (Devens, MA)
- …and implements procedure and forms to assure compliance with current practices or GMP trends. + Provides support to the supplier development team preparing quarterly ... + Demonstrated hands on supplier management implementation in regulatory agencies like: FDA , ANVISA, COFEPRIS, EMEA, BfArM, JP, MHRA among others. + Ability to… more
- Charles River Laboratories (Boston, MA)
- …by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment. ... worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your… more
- Charles River Laboratories (Boston, MA)
- …by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment. ... worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your… more