- ZOLL Medical Corporation (Pawtucket, RI)
- …+ Bachelor's Degree in Engineering or technical discipline required + 5 Years medical device experience required Knowledge, Skills and Abilities + Proficient ... compliance with ISO 14971 * Develop and implement quality plans * Ensures post market surveillance reviews are...of commonly used concepts, practices, and procedures related to medical device manufacturing + Working knowledge of… more
- Terumo Medical Corporation (Elkton, MD)
- …or similar. + Requires six to ten years increasing responsibility and experience in a medical device quality assurance environment. + Prefer one to two years ... develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- Terumo Medical Corporation (Somerset, NJ)
- …Compliance , or other related Quality System role(s) in a medical device or pharmaceutical company + Experience performing root cause ... US, 08873 Company: Terumo Medical Corporation Department: Quality Systems & Compliance **Job Summary** The...+ Knowledge in 21 CRF Part 820, ISO 13485:2016, Medical Device Directive / Regulation. + Strong… more
- Stryker (Portage, MI)
- …Assurance** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... or Computer Science. + Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601), with experience in… more
- Abbott (Alameda, CA)
- …relate to the development, verification, validation, and maintenance of application in support of medical device software. + Software Quality lead in various ... they apply to the development, verification, validation, use, and maintenance of medical device software. + Coordinate activities with other engineering… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- … Audits to assure compliance with domestic and international medical device standards and regulations, local procedures, and corporate policies/procedures. ... assigned. She/he functions as a subject matter expert for quality and compliance issues. **Job Description** We...Minimum 10 years of experience work experience in the Quality organization of a Medical Device… more
- J&J Family of Companies (Santa Clara, CA)
- …+ Bachelor's degree and 10+ years of quality related experience in the Medical Device industry + Excellent working knowledge of current USA Food and Drug ... Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated… more
- Integra LifeSciences (Plainsboro, NJ)
- …Chemical, or Electrical) + Experience: 3 to 6 years of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing. + ... The ** Quality Assurance Engineer II** will provide Quality compliance support on all aspects of...and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical… more
- J&J Family of Companies (Titusville, NJ)
- …strong track record of talent development. * Prior experience in the pharmaceutical and/or medical device industry. * Knowledge of sales, marketing, medical ... management. * Experience with FDA advertising and promotional practices for pharmaceutical/ medical device products. Skills Required: * Exceptional written and… more
- Abbott (Alameda, CA)
- …combination of education and work experience + Minimum 8 years' experience in the medical device industry, with 5 of those years related to the preparation ... level degree + Experience with FDA, ANVISA, TGA, NMPA, EU and other international medical device / drugs / pharma regulations and submissions. + Experience with… more
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