- Editas Medicine (Cambridge, MA)
- …Editas Waltham and Editas Devens GMP manufacturing facilities. Key Responsibilities: As the Principal Specialist , you will be responsible for: + Support Editas' ... life science and 8+/6+ years respectively of relevant industry experience in Quality Assurance in a Pharmaceutical/Biotech GMP environment. + Experience… more
- Medtronic (Boston, MA)
- …prompt and effective manner + Report and device complaints to proper departments within quality assurance within Medtronic + Help drive and maintain quality ... THAT CHANGE LIVES - POSITION DESCRIPTION:** The CoreValve Therapy Development Specialist provides technical, clinical, educational and sales support to ensure safe… more