- AbbVie (Irvine, CA)
- …in conducting R&D projects + Experience and working knowledge of medical device , drug and/or biologics, and combination product regulations (21 CFR 820, 21 ... in vivo and tissue processing methods to support development of novel medical device /tissue products. + Critically evaluate scientific or regulatory advances,… more
- BD (Becton, Dickinson and Company) (Durham, NC)
- …and a collaborative mindset are key, as is a deep understanding of US medical device regulations and current European quality system standards, including MDD ... + Minimum 3 years of Regulatory Affairs experience in medical device or in vitro diagnostic ...device and in vitro diagnostic areas + International product registration experience preferred Click on Apply if this… more
- Terumo Medical Corporation (Somerset, NJ)
- …is required. **Knowledge, Skills and Abilities (KSA)** + Working knowledge of medical device industry contracting, including knowledge of standard business ... Hospital/Institutional, and/or other sales-based contracts and contracting processes. + Medical device and/or pharmaceutical contracting experience preferred,… more
- Fresenius Medical Center (Lawrence, MA)
- …for staffing and leading a team of software developers to deliver high quality medical device software. Develop and drive a long-term strategic vision for the ... in software development, verification, and standards necessary to meet global medical device regulatory requirements. + Clear understanding of Software… more
- Stryker (Fort Wayne, IN)
- …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 engineering. + Minimum of 4 years of professional experience in the highly regulated medical device industry, with a focus in one or more of the following… 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
- Lilly (Indianapolis, IN)
- …A minimum of 2 years of work experience in GMP regulated pharmaceutical and/or medical device industries is required. + Background in sterile barrier and/or deep ... + Broad integrated technical knowledge for system and design engineering, product development, and commercialization of pharmaceuticals, medical devices,… more
- BD (Becton, Dickinson and Company) (Covington, GA)
- …advanced manufacturing engineering, product design, and/or technical leadership level in Medical Device or other highly regulated industries. OR5+ years of ... Leader for UCC, the incumbent shall provide a leading Product & Process Design role in planning and execution...& Process Design role in planning and execution of medical device projects for the Urology and… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- …engineering (MedTech industry preferred) + Consistent track record of leading complex medical device development from concept to market + Strong knowledge ... of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to...of regulatory requirements and quality standards in the medical device industry (FDA, ISO 13485, ISO… more
- 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 ... stay updated on the SUT/CAD VAT rules within the medical device industry for multiple jurisdictions. This...jurisdictions (Nexus) are identified and maintained. + Collaborate with product managers to gain insights into current and future… more