- Terumo Medical Corporation (Somerset, NJ)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... of direct market research and/or marketing analytics experience, preferably in the medical device manufacturing industry; or equivalent combination of education,… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... data analysis and executes experiments to qualify or resolve product and process issues. 8. Creates, reviews, and approves...CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO 14971, ISO 13485,… more
- Abbott (Alameda, CA)
- …discipline. + Must have 5+ experience in Software Quality Assurance. + Knowledge of medical device standards including FDA QSR, ISO 13485, ISO 14971, 21 CFR ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Maple Grove, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...+ Procedural Writing + Regulatory Change Assessment + International Product Registration support + Ad and Promotional Material -… more
- Globus Medical, Inc. (Audubon, PA)
- …them with the necessary tools, knowledge, and skills to excel in a competitive medical device market. The ideal candidate will have a strong background in ... initiatives + Work closely with sales leadership, marketing, and product teams to ensure training content is current, relevant,...of 2 years of sales training, preferably within the medical device industry + Medical … more
- Caldera Medical (Columbus, OH)
- …who is looking to develop a sales career in the competitive arena of medical device sales. You'll be responsible for contacting and interacting with current ... and potential customers, identifying their needs, leading product trials in the operating room and persuading surgeons...? Caldera Medical is a growth stage medical device company dedicated to improving the… more
- Caldera Medical (Westlake Village, CA)
- …and regulatory requirements. * Ensure timely and accurate complaint evaluations, including medical device reporting (MDR) or equivalent regulatory submissions. * ... complaints and working on CAPA. * Bachelor's degree preferred. * Experience working within medical device industry and familiarity with 21 CFR 820, and ISO 13485… more
- LSI Solutions (Victor, NY)
- …in 1986, located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive ... We are searching for passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R) an ISO 13485 certified company,… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …to understand the appropriate legal and regulatory requirements in the areas of medical device operations and to establish robust processes and controls to ... discipline. required + Experience in an FDA regulated Class III electrical medical device manufacturing environment preferred.preferred and + Experienced in… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... degree with 2+ years of related quality experience. + Experience with Medical Device Complaint handling, Post Market Surveillance and Regulatory reporting… more