- TE Connectivity (Wilsonville, OR)
- … business unit is a leader in engineering design and manufacturing within the medical device industry. Specializing in critical components such as metal shafts, ... design specifications, test plans and qualification reports. Ensure compliance with relevant medical device regulations and quality processes. * Mentorship: Act… more
- Kestra Medical Technologies, Inc (Kingsport, TN)
- …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 ... skill for pressure situations. Requirements Education/Experience Required: * 5+ years of successful medical device sales experience * 3+ years of outside sales… more
- Kestra Medical Technologies, Inc (San Bernardino, CA)
- …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 ... skill for pressure situations. Requirements EDUCATION/EXPERIENCE REQUIRED: + 5+ years of successful medical device sales experience + 3+ years of outside sales… more
- ZOLL Medical Corporation (Chelmsford, MA)
- …this role ensures legal integrity while supporting innovation in the company's medical device businesses.Essential Functions + Strategy -Implement the overall ... outside counsel for the company. Ensure adherence to applicable regulations, international medical device standards and healthcare laws including HIPAA and… more
- Amazon (Sunnyvale, CA)
- …The solutions we develop determine which AI features can be offered on- device versus requiring cloud connectivity, ultimately shaping product capabilities and ... Description Our team leads the development and optimization of on- device ML models for Amazon's hardware products, including audio, vision, and multi-modal AI… 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 ... of direct market research and/or marketing analytics experience, preferably in the medical device manufacturing industry; or equivalent combination of education,… 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
- 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 ... Quality System Regulations, 21 CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO 14971, ISO 13485, and MDD 93/42/EEC +… more
- Teleflex (Wyomissing, PA)
- …and validation execution of microbiological and biological test methods for medical device evaluation. This role requires advanced laboratory expertise, ... Demonstrated experience working within quality-regulated environments (FDA, ISO standards) in medical device , biotech, or pharmaceutical industries. * Prior… more
- AbbVie (Orlando, FL)
- …performance selling teams to maximize coverage to targeted customers. The SAM provides technical product and procedure expertise, as well as, competitive ... skin resurfacing equipment, 2) topical skincare consumables designed for the resurfacing device and 3) SkinMedica product portfolio. Must collaborate with Facial… more