- Edwards Lifesciences (Irvine, CA)
- …in related field, 5 years experience quality and/or manufacturing environment in the medical device industry **OR** equivalent work experience based on Edwards ... Functions as an integrator between the business users, IT and corporate compliance with both business and technical expertise. **How You'll Make an Impact:**… more
- Terumo Neuro (Aliso Viejo, CA)
- …(12) years of related work experience, including minimum six (6) years of medical device industry experience 3. Strong written and verbal communication skills ... EMC, etc.) 9. Work with regulatory stakeholders to identify all compliance requirements for medical devices with electronics 10. May be required to guide,… more
- Stryker (Memphis, TN)
- …NIST, ISO, and related security frameworks, particularly in vulnerability management. + Knowledge of medical device regulations (eg, US FDA 21 CFR Part 820, ISO ... development from concept to launch, ensuring patient safety, product security, and compliance with global standards. Your expertise will drive innovation and quality… more
- WM (Columbia, MD)
- …a US based business-to-business services company and leading provider of compliance -based solutions that protects people and brands, promotes health and well-being, ... ago, we have grown from a small start-up in medical waste management into a leader across a range...US based business-to-business services company and leading provider of compliance -based solutions that protects people and brands, promotes health… more
- Cella Inc (Lake Forest, IL)
- …5+ years for Senior roles) working within the pharmaceutical, biotech, or medical device sectors. A comprehensive understanding of promotional material review ... involves precise coordination and sign-off from cross-functional teams, including Medical , Legal, Regulatory, Compliance , and Commercial stakeholders.… more
- Sanofi Group (Chicago, IL)
- …four-year college or university. + 3 years minimum of pharmaceutical, biotech, or medical device sales experience. + Demonstrated ability to learn and apply ... integrity strictly following all Sanofi Genzyme US policies and in compliance with all policies and procedures governing the promotion of pharmaceutical/biological… more
- BayCare Health System (Tampa, FL)
- …closely with radiation oncologists, physicists, and therapy teams and maintain compliance with safety, quality assurance, and regulatory standards throughout all ... densities, and anticipate issues affecting plan quality and robustness. + ** Device & Immobilization Support:** Assist in designing, fabricating, and verifying… more
- BD (Becton, Dickinson and Company) (Madison, GA)
- …(Associates or Bachelor's degree preferred) + Preferred three years of experience in medical device or GMP regulated environment with process validation of ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...maintenance of the validation temp/RH monitoring equipment. + Ensures compliance to divisional, Corporate, ISO, and EN requirements. +… more
- ARTIDIS (Houston, TX)
- …to individual patients' needs and desired outcomes. Job Purpose ARTIDIS is a medical device start-up company that conducts clinical studies to validate and ... develop new cases for its medical products. Given that ARTIDIS's medical devices...study processes with emphasis on quality assurance, quality control, compliance and auditing. Duties and Responsibilities + Monitors the… more
- Guidehouse (Philadelphia, PA)
- …Life Sciences practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle ... your DNA? Breakthroughs in pharma are helping people live healthier lives, while medical devices enable patients to proactively maintain health - this is undoubtedly… more
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