- Regeneron Pharmaceuticals (East Greenbush, NY)
- …experience: + Associate Director: 10+ years of experience in the pharmaceutical or medical device industry or equivalent combination of education and experience. ... + Director: 12+ years of experience in the pharmaceutical or medical device industry or equivalent combination of education and experience. Does this sound like… more
- Kestra Medical Technologies, Inc (Tampa, FL)
- …Kestra team has over 400 years of experience in the external and internal cardiac medical device markets. The company was founded in 2014 by industry leaders ... the care team of process and training for patient compliance and experience. . Link the SWO renewal process...or business . Minimum 2 years industry experience in medical device , pharmaceuticals, or a comparable healthcare… more
- US Tech Solutions (San Bruno, CA)
- …Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation ... and support CAPA, complaints, audits, and overall QMS functions. **Experience:** ** Medical Device Software Experience:** 1. Proven experience in software… more
- UnityPoint Health (Grimes, IA)
- …and processes medical equipment documentation to create knowledge articles, manage medical device profiles in CMMS and/or other integrated toolsets, and ... support to field leaders, technicians and the business for escalated issues related to medical device security. . Monitors intelligence sources for medical … more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …our international regulatory team in further launch activities. The ideal candidate will have medical device and in vitro diagnostic experience in the US and EU, ... engineering, bioengineering, biology, chemistry). + Minimum 5 years Regulatory Affairs experience in medical device or in vitro diagnostic device companies… more
- Merck (Rahway, NJ)
- …& standards:** + 21 CFR Part 4 + 21 CFR 820 + 21 CFR 210/ 211 + EU Medical Device Regulation + USP <1> + USP <697> + FDA Guidance for Industry, Container Closure ... Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Microscopies, Negotiation, Optical… more
- CAI (Plymouth, MN)
- …Summary** As an Assembly Operator, you will be responsible for assembling various medical device components and products according to strict procedures and ... US as a refugee. **What** **You'll** **Do** + Assemble medical device components and products according to...+ Perform visual inspections and quality checks on assembled medical products, ensuring compliance with stringent … more
- Olympus Corporation of the Americas (Center Valley, PA)
- …(https://www.olympusamerica.com/careers) . **Job Description** Responsible for the review of medical device global complaints and coordinate the resolution ... Latin America, Japan, and others). The Analyst III is responsible for determining medical device reportability for Olympus products or products for which Olympus… more
- Veterans Affairs, Veterans Health Administration (Miami, FL)
- …to determine expectations, lifestyle, home/work environment, ability to use the device . Takes necessary measurements, casts or scans to develop positive molds ... to accommodate or treat a wide range of complex medical conditions, which include unusual problems or complications. Considering...and components to be used in fabrication of the device and determines appropriate equipment to be used in… 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 ... replacement of various types of facilities infrastructure in support of a medical device cleanroom manufacturing facility. The primary responsibility is to… more