- Beckman Coulter Diagnostics (Miami, FL)
- …regulations and standards including compliance with Food & Drug Administration (FDA), Medical Device Single Audit Program (MDSAP), ISO13485, European Union ... Medical Device Directives (MDD), and In-Vitro Medical ...with 9+ years of experience, preferably in areas of medical devices, engineering , or quality assurance.Strong knowledge… more
- Cytiva (Miami, FL)
- …3-5 years of experience in a process engineering or project engineering role, preferably in healthcare manufacturing or medical device production.2+ ... in a regulated environment. The ideal candidate will have experience in process engineering , project management, and a strong understanding of healthcare… more
- Raytheon (Mckinney, TX)
- …We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's ... tough, meaningful problems that create a safer, more secure world. Tool Engineering is a career field that specializes in designing custom mechanical solutions… more
- Cytiva (Miami, FL)
- …Quality Engineering , or Manufacturing Operations within Life Sciences, Biotechnology, Medical Device , Biopharma, or other FDA or EPA-regulated manufacturing ... & Advocacy: Collaborate with site and global leadership to address process changes, advocate for site-specific needs, and drive customer-centric solutions during… more
- Cytiva (Miami, FL)
- …walks.It would be a plus if you also possess previous experience in: Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949Speaking fluent ... discovery to delivery. What you will do:Supplier qualification, including supplier process qualification (SPQ) for Type I (critical) supplier.Manage the supplier… more
- Cytiva (Miami, FL)
- …walks.It would be a plus if you also possess previous experience in: Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949#LI-OnsiteJoin our ... from discovery to delivery.What you will do:Supplier qualification, including supplier process qualification (SPQ) for Type I (critical) supplier.Manage the supplier… more
- Raytheon (Andover, MA)
- …We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's ... initiatives to go above and beyondRelentlessly interact with a team of process engineers, technology owners, and project leadsProduce key reliability metrics such as… more
- Cytiva (Miami, FL)
- …of experience in Quality or Regulatory in a regulated industry (ISO 9001, medical device , or pharmaceutical preferred).Experience with root cause analysis, CAPA ... manufacturing and design, ensuring compliance with regulatory standards and driving process improvements; leading root cause analysis and CAPA initiatives, ensuring… more
- Beckman Coulter Life Sciences (Indianapolis, IN)
- …experience in product development, manufacturing and / or quality systems (ISO 9001), medical device (ISO 13485), pharmaceutical, related life sciences or other ... Risk Management (per ISO 14971), Production, Service Controls. Assuring compliant process and product documentation, inclusive of Design History, Product, Process… more
- dsm-firmenich (Exton, PA)
- …+ 3-5+ years experience as engineer preferably in process safety engineering , chemical operations, medical device , chemical operations, or associated ... ** Process Safety Engineer** **Wayne, PA/Exton, PA** The ...equipment. Prepare documentation to provide sufficient information for Project Engineering for detailed specifications for cost estimates and construction.… more
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