- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …is preferred Experience + At least 3 to 5+ years' work experience ( IVD , Medical Device, Pharmaceutical or consulting experience is preferred) + Business experience ... may include marketing, sales, sales training, business development Knowledge, skills and abilities + Proactive self-starter with the ability to thrive in a fast-paced, dynamic environment + Strong action orientation with excellent prioritization and… more
- Abbott (Alameda, CA)
- …CFR 820, ISO 13485, the Medical Devices Directive (93/42/EEC) and/or the IVD Directive (98/79/EC). Preferred Qualifications . 5 years' experience working with Class ... II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. . Experience with 510(k) applications, PMA supplements, US device regulations, and/ or with EU and other international medical device regulations and… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …and clinical labs sourcing, negotiations and contracting. Experience with IVD regulations and requirements. Knowledge regarding rates, unit costs, costing ... structures, cost models, and TCO. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health… more
- Danaher Corporation (New Brighton, MN)
- …include: + 2-5 years of relevant experience within the Medical Device or IVD industry is required. + Expertise in statistical analysis software (JMP/Minitab, etc.) ... and methods is vital. + Strong Problem Solving skills and ability to get plans into actions is required. + Prior experience in the area of biomedical or blood gas sensor design and development is desired. Travel, Motor Vehicle Record & Physical/Environment… more
- Danaher Corporation (Richmond, IL)
- …technical field and 5+ years' experience with increasing responsibility in medical device/ IVD + Experience working within a medical device quality system in ... compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations + Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues + Track record of… more