- Actalent (Jackson, WI)
- …regulatory product registrations, and facility registrations. + Oversee medical device document management, internal investigations (including Deviations and CAPAs), ... quality assurance. + Experience in OTC, pharmaceuticals, and medical devices . + Knowledge of GMP, FDA, and OTC regulations....+ 5 years of experience in OTC, Drug, Medical Device , or Cosmetics. + Experience with FDA and cGMP… more
- US Tech Solutions (IL)
- …+ Take part in **post-market safety surveillance** activities for assigned medical devices and contribute to area projects and objectives. Identify issues and ... as necessary. + Conduct medical safety assessments (MSA) for medical device complaints involving reported adverse events and, occasionally, technical events. +… more
- Integra LifeSciences (Princeton, NJ)
- …changes with corporate and international regulatory teams. + Lead Unique Device Identification system requirements and other labeling compliance of new products ... experience in an FDA regulated industry such as Medical Devices , Biotech or Pharma (must have at least 2...+ Strong working knowledge of domestic and/or international medical device regulations including 510k, PMA, PMA Supplements,361 HCT/Ps, and… more
- Actalent (Maple Grove, MN)
- …delivery catheter system. This position requires a background in the medical device industry, particularly in cardiological devices , including implantable heart ... experience. + 8+ years of experience in the medical device industry with 3 to 5 years in Quality....Deep understanding of CE Marking, EU MDR, FDA Medical Device Regulation (MDR), and FDA requirements. + Extensive knowledge… more
- Actalent (Minneapolis, MN)
- …manufacturing functions, requiring deep familiarity with catheter-based medical devices , early-phase development, design controls, and cross-functional leadership. ... clear, data-driven communication. Essential Skills + 5+ years experience in medical device development as a Project Manager or Senior Engineer, ideally with… more
- Medtronic (Denver, CO)
- …and familiarity with key literature. + Has a solid understanding of competitive lateral devices in the US + Adheres to company policies and conducts all business in ... and 8+ years of relevant sales, clinical, or related experience in medical device , Medtech, healthcare or life sciences; or + Associates Degree and 6+ years… more
- Philips (Plymouth, MN)
- …manufacturing indicators, CAPAs, HHAs, etc. Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. + Serving as SME ... years of experience in Software Quality and/or Software Development in medical device industry with hands on experience with SW Design verification and/or… more
- Robert Half Technology (San Diego, CA)
- …complex technical issues across cloud services, Microsoft 365 ecosystem, and endpoint devices . + Support device management and compliance using Intune across ... infrastructure, and cloud integrations. + Implement and support Conditional Access, device compliance, MFA, and identity management policies in Azure. + Integrate… more
- LSI Solutions (Victor, NY)
- …located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive surgical ... are searching for passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R) an ISO 13485 certified company, you will… more
- LSI Solutions (Victor, NY)
- …located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive surgical ... are searching for passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R) an ISO 13485 certified company, you will… more