- Beckman Coulter Diagnostics (Miami, FL)
- …experience or Doctoral degree with 9+ years of experience, preferably in areas of medical devices, engineering , or quality assurance.Strong knowledge of ... regulations and standards including compliance with Food & Drug Administration (FDA), Medical Device Single Audit Program (MDSAP), ISO13485, European Union … more
- Cytiva (Miami, FL)
- … Engineering , or Manufacturing Operations within Life Sciences, Biotechnology, Medical Device , Biopharma, or other FDA or EPA-regulated manufacturing ... of leadership experience, with senior leadership roles in QA, Operations, or Quality Engineering preferred.Regulatory and Quality Expertise: Strong knowledge… more
- Cytiva (Miami, FL)
- …in Quality or Regulatory in a regulated industry (ISO 9001, medical device , or pharmaceutical preferred).Experience with root cause analysis, CAPA ... career.Learn about the Danaher Business System which makes everything possible.The Quality Assurance Engineer (Design & Manufacturing) is responsible for providing … 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 ... about the Danaher Business System which makes everything possible.The Senior Supplier Quality Engineer (m/f/d) for Cytiva is responsible to manage supplier defects,… 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 ... about the Danaher Business System which makes everything possible.The Senior Supplier Quality Engineer for Cytiva is responsible to manage supplier defects, be… more
- Beckman Coulter Life Sciences (Indianapolis, IN)
- …required.BS+7 or MS+4 years' experience in product development, manufacturing and / or quality systems (ISO 9001), medical device (ISO 13485), ... about the Danaher Business System which makes everything possible.The Staff Quality Assurance Engineer or Scientist is responsible for facilitating application of… more
- Cytiva (Miami, FL)
- … or project engineering role, preferably in healthcare manufacturing or medical device production.2+ years experience with regulatory standards and ... manufacturing processes, managing projects, and ensuring the efficient production of high- quality medical devices and products in a regulated environment.… more
- Raytheon (Tucson, AZ)
- …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 ... complex systems. Our precision software and firmware integrate operating systems, device drivers, networking, and control software to bring together sensor,… more
- Actalent (Irvine, CA)
- …on quality system requirements, quality tools, and best practices. Skills Quality engineering , Medical device , Root cause analysis, Quality ... management, documentation review Top Skills Details Quality engineering , Medical device ,Root cause analysis Additional Skills & Qualifications… more
- Kelly Services (Deerfield Beach, FL)
- …during all development and manufacturing stages. **Requirements** + 5+ years Quality Engineering in Medical Device or Pharmaceuticals + Knowledge of ISO ... and actively cooperates with multiple departments. **Responsibilities** + Represent Global Quality Engineering in all Design Controls and Product Development… more
- Kelly Services (Santa Clara, CA)
- … Quality Engineer_** _for a long-term contract at one of our_ **_Global Medical Device Robotics & Digital Solutions_** _clients in_ **_Santa Clara, CA_** _. ... this group you will be eligible for 50% paid Medical & Dental, a 401K plan, and a variety...will play a critical role in supporting the system quality engineering team._ _Medical Device_ **_Design … more
- Abbott (Santa Clara, CA)
- …field. + 2-3 years (+) experience in Quality Assurance/ Quality Engineering from medical device or pharmaceutical industry. + Sufficient knowledge ... experience in relevant areas of Quality , Regulatory or Engineering , preferably within a medical device environment + Advanced knowledge of relevant… more
- Terumo Neuro (Aliso Viejo, CA)
- …Minimum of six (6) to eight (8) years of quality or manufacturing engineering experience in medical device or other regulated manufacturing industry. 3. ... **12580BR** **Title:** Staff Engineer, Quality Engineering (Transfers) **Job Description:** Lead...risk analysis, and change control. 2. Strong knowledge of medical product quality assurance (including the requirements… more
- BD (Becton, Dickinson and Company) (Tempe, AZ)
- …**Position Summary:** Primary focus of this position is to assist Quality Engineering activities for medical device process development, design controls, ... device post-market analysis 10. Provide summary reports to quality engineering on status of deliverables. 11....Associates of Science degree in a technical field + Medical device or other regulated FDA/QSR and… more
- Zimmer Biomet (Warsaw, IN)
- …of Quality (ASQ) preferred. + 5-7 years experience in a Quality Engineering role; Medical device strongly preferred, or an equivalent combination of ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...(suppliers, regulatory agencies, etc.). + Facilitates team efforts on quality engineering projects. + Ability to deliver,… more
- Philips (WA)
- …acquired 10+ years of experience in manufacturing, quality , or procurement engineering ( medical device industry/regulated industry - highly preferred) ... suppliers using Supplier Corrective Action Request (SCAR) and Six Sigma Quality Engineering toolsets. + Planning and executing supplier quality performance… more
- Caldera Medical (Westlake Village, CA)
- …or related field), and a minimum of 5-7 years of experience in Quality Engineering in a regulated medical device or pharmaceutical industry. Or * ... a minimum of 2-5 years of experience in Quality Engineering in a regulated medical device or pharmaceutical industry. Certifications: * Six Sigma Green… more
- GE HealthCare (Chicago, IL)
- …Minimum of 2 years of work experience in quality assurance or quality engineering in a medical device organization. + Legal authorization to work in ... **Job Description Summary** This position will support the Chicago Quality Organization by implementing and upholding GEHC Quality...+ Good understanding and knowledge of local and global Medical Device QMS regulations and standards such… more
- Olympus Corporation of the Americas (Westborough, MA)
- …+ Minimum 10 years of experience in Supplier Quality or Quality Engineering in the Medical Device Industry. + Experience leading and managing direct ... with company policies specifications procedures and medical device regulations. The Director of Supplier Quality ... device regulations. The Director of Supplier Quality will partner with Manufacturing Engineering Operations… more
- Actalent (Irvine, CA)
- …and third party audit activities. Essential Skills + Experience in quality engineering within the medical device industry. + Proficiency in TrackWise ... related field. + Minimum of 3-5 years of experience in quality engineering within the medical device industry. + ASQ Certified Quality Engineer (CQE)… more
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