- Medtronic (Santa Rosa, CA)
- …discipline + Minimum of 7 years of direct Regulatory Affairs experience within the medical device or other regulated industry, + Or advanced degree with a ... healthcare forward and remain a global leader in medical technology and solutions. This role will be based...minimum of 5 years of Regulatory Affairs experience. + Medical device industry experience with Class I/II/III/IV… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …professional to join our team in a critical role ensuring product safety and compliance in the medical device industry. **Responsibilities** + **Lead ... and maintaining the Post - Market Surveillance program in compliance with EU MDR, EU IVDR, Health Canada, China...safety **Skills** + **Regulatory Knowledge:** Extensive understanding of FDA medical device regulations (21 CFR Part 820),… more
- Teleflex (Morrisville, NC)
- …* Additional experience in clinical setting, biostatistics, IDE clinical studies or medical device product support. * Demonstrate aptitude in and knowledge ... outside of Philadelphia in Wayne, PA. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a… 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 ... Req ID: 5161 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: QM Laboratory Ops Terumo Medical...broad range of applications for numerous areas of the healthcare industry. TMC places a premium on providing customers… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device ... work that creates change and shapes the future of healthcare . Thinking differently is what we do best. To...and Drug Administration (FDA) regulations, ISO 9001, ISO 13485, Medical Device Directive (MOD), the Canadian … more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device ... work that creates change and shapes the future of healthcare . Thinking differently is what we do best. To...and Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian … more
- Mount Sinai Health System (New York, NY)
- …This position ensures consistent supply charging practices across departments and facilities, compliance with clinical research and free device set-ups, and the ... to ensure timely, accurate and compliant recording of hospital device -related revenue and maintenance of the CDM for all...of EHR Software, EPIC + CDM Coding skills understands Healthcare Common Procedure Coding System (HCPCS) for supplies. +… more
- ThermoFisher Scientific (Greenville, NC)
- …supplying medical information services to our customers, patients and healthcare providers. We engage with healthcare professionals, regulatory agencies and ... pharmaceutical customers to help them navigate regulatory and compliance requirements around the world. We manage medical information inquiries, document adverse… more
- Medtronic (Minneapolis, MN)
- …the following tasks: + Product Security - Implement security requirements across the medical device development lifecycle by collaborating with teams to uphold ... and the use of Hardware Security Modules (HSMs) for medical device protection. + Use of advanced...device software and systems + Security Standards & Compliance - Ensure the implementation and maintenance of security… more
- Integra LifeSciences (Princeton, NJ)
- …Engineer II with a focus on bacterial endotoxin testing programs in the medical device industry. The successful candidate will be responsible for partnering ... work that creates change and shapes the future of healthcare . Thinking differently is what we do best. To...learn about bacterial endotoxin testing programs, an understanding of medical device quality systems, and a commitment… more