- PCI Pharma Services (Rockford, IL)
- …Validation Engineer** to support the validation activities associated with medical device assembly lines within a fast-paced Contract Development and ... shape the future of PCI. **Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)** **Location:** [Rockford] **Department:** Quality **Reports… more
- Medtronic (Northridge, CA)
- …management framework, ensuring compliance with ISO 10993 standards and global medical device regulations. This role involves conducting comprehensive ... related fields. MS or PhD preferred. + Strong understanding of ISO 10993 and global medical device regulations (eg, EU MDR, FDA, REACH, Prop 65). + Experience… more
- Cook Medical (Bloomington, IN)
- … clinical , and regulatory affairs.- Provide leadership in the understanding of medical device regulations and best practices.- Manage conflict resolution as ... Qualifications - Engineer degree and 5-8 years of experience- Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and risk management (ISO… more
- Cook Medical (Ellettsville, IN)
- … clinical , and regulatory affairs.* Provide leadership in the understanding of medical device regulations and best practices* Manage conflict resolution as it ... Qualifications * Bachelors degree in a scientific discipline* Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and risk management (ISO… more
- Zimmer Biomet (Englewood, CO)
- …or related engineering discipline with 6+ years of experience + Prior experience in medical device development required. + Prior experience in taking a ... and renewed life to people around the world. To support our talented team, we focus on development opportunities,...medical device or similar product from ideation… more
- Bon Secours Mercy Health (Lima, OH)
- …the prescribed medication ordered by the physician and adjusting the machine or device to accomplish patient's individual clinical needs; document and observe ... effectiveness. Our hospitals, care sites and clinicians are recognized for clinical and operational excellence. **$10,000 Sign On Bonus** **Mercy Health** **_Intro… more
- DEKA Research & Development (Manchester, NH)
- …for a Biocompatibility & Toxicology Senior Scientist to join our team focused on medical device and combination product development. The individual in this role ... the organization stays up to date on global regulatory changes to medical device biocompatibility standards and requirements through monitoring regulatory… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Science or other relevant engineering/technical degree and 10 years' experience in the medical device industry or a Master's Degree and 8 years' experience… more
- UTMB Health (Galveston, TX)
- …cardiovascular perfusion training program. The ES is responsible for the coordination of clinical care for patients requiring the support of extracorporeal life ... cables, or ECMO system components, ensuring minimal interruption of support . KNOWLEDGE/SKILLS/ABILITIES . Satisfactory maintenance of clinical competencies… more
- Gilead Sciences, Inc. (Foster City, CA)
- …communication skills are required. + Demonstrated ability to facilitate the interface with medical device vendors and HF consulting firms. + Demonstrated ability ... device combination product design and development from feasibility, clinical development, through registration, and post-market. This includes requirements… more