- Zimmer Biomet (Dover, OH)
- …policies and procedures, the Quality System Regulation (21 CFR Part 820), ISO 13485, the Medical Device Directives (MDD), Medical Device Regulation (EU ... Audit or ASQ certifications such as RABQSA, CQA, CQE are strongly preferred. + Medical Device regulations knowledge and experience is required. + FDA or Notified… more
- Cordis (Irvine, CA)
- …* Bachelor's Degree in a Scientific or Engineering Discipline * Experience with current medical device regulations in the EU, US, and Asia. * 10+ years ... environmental monitoring, to ensure methods used for bioburden and sterilization monitoring are robust and compliant to the relevant...of experience in Class II or III Medical Device Quality Management * 5+ years… more
- J&J Family of Companies (San Lorenzo, PR)
- …skills. **Preferred:** + Experience in the Medical Device industry or medical field. + ASQ Certified Quality Auditor (CQA) or ISO Certified Lead ... to all Site functions and directly supervises Quality Laboratory Supervisors, Sterilization SMEs, Quality Engineers, Quality Team Leaders, Quality Systems Team… more
- Medtronic (North Haven, CT)
- …action (CAPA/SCAPA) + High-level Supplier Change request knowledge + Mastery of medical device quality systems and applications is required + Demonstrated ... plant operations preferred + Design Control knowledge preferred + Knowledge of sterilization methods preferred + Thorough understanding of the US and international… more
- BD (Becton, Dickinson and Company) (Columbus, NE)
- …of 10 years of experience in a manufacturing environment. + Experience in Medical Device , Chemical, or Pharmaceutical manufacturing is preferred. + Experience ... and Safety programs for Pharmaceutical Systems and NAMc, including sterilization unit in compliance with BD corporate and local...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more
- Integra LifeSciences (Plainsboro, NJ)
- … medical devices in conformance with the Quality System Regulation, ISO 13485, Medical Device Directive, ISO 14971, IEC 60601 and other regulatory standards. ... + BS in Engineering or associated scientific discipline. + Minimum 5 years Medical Devices or Pharmaceutical experience in Quality or R&D Engineering position. +… more
- Medtronic (Billerica, MA)
- …metal precision processing, and adhesives for the Catheter/Disposable SQE position. + Medical device manufacturing industry experience, preferably ISO 13485. + ... the only way to drive healthcare forward and remain a global leader in medical technology and solutions. **A Day in the Life** Medtronic is currently searching for… more