- Kelly Services (Deerfield Beach, FL)
- …and standards during all development and manufacturing stages. **Requirements** + 5+ years Quality Engineering in Medical Device or Pharmaceuticals + ... and applicable regulations. + Support Risk Management activities for medical devices and the device part of...device combination products for products are of high quality and directs product development decisions by promoting a… more
- PDS Tech Commercial, Inc. (Gainesville, FL)
- …| Gainesville, FL** _6-Month Contract with a Global Leader in Medical Device Manufacturing_ **Make an Impact Where Quality Meets Innovation** PDS Tech ... Commercial is proud to partner with a world-renowned medical device manufacturer in Gainesville, FL. We...goals. + Perform all work in accordance with strict quality , safety, and compliance standards. + Collaborate with team… more
- Stryker (Orlando, FL)
- …Assurance** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... strong technical skills + Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601), with experience in… more
- Otsuka America Pharmaceutical Inc. (Tallahassee, FL)
- …degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of current global Good ... an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will...Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with… more
- Medtronic (Jacksonville, FL)
- …world. **A Day in the Life** **Careers that Change Lives** Our space, the medical device and healthcare industry, is rapidly changing. It always has been ... years relevant experience. **To Be Successful in this role:** + Experience in the medical device , in-vitro diagnostics or pharma industries + Strong knowledge of… more
- Terumo Aortic (Sunrise, FL)
- …Affairs Laws, the Canadian Quality System Regulation, MDSAP and the Medical Device Regulation (MDR). Job Details: + In all actions, demonstrate ... with FDA, ISO 13485, EU MDR, MDSAP and global quality system requirements for medical devices. + Strong analytical skills including trend and statistical… more
- Danaher Corporation (Pensacola, FL)
- …or technical field required + 1+ years of relevant experience in biomedical or medical device manufacturing preferred + Uses analytical mind and data analysis ... Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Quality Engineer is responsible for ensuring the quality… more
- Danaher Corporation (Miami, FL)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Familiarity with ISO13485, 21 CFR Part 820, ... System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Global Supplier Quality Engineer - Systems and Innovation for Beckman Coulter… more
- Danaher Corporation (Miami, FL)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Certifications such as CQE, CQA, Six Sigma, ... System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will… more
- Danaher Corporation (Pensacola, FL)
- …or technical field required + 3+ years of relevant experience in biomedical or medical device manufacturing preferred + Uses analytical mind and data analysis to ... Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Quality Engineer is responsible for ensuring the quality… more