- Medtronic (Northridge, CA)
- …Technical degree is a plus. + Experience with Design Control documentation within medical device industry or Pharma industry. + Experience conducting and ... of initiative and self-motivation. + Prior work experience in a regulated industry ( Medical Device Industry preferred) + Sound experience and through knowledge… more
- Integra LifeSciences (Plainsboro, NJ)
- …US. Food and Drug Administration Regulations, ISO 9001, ISO 13485:2016 Standard, European Medical Device Directives, Canadian Medical Device Regulations, ... outcomes and set new standards of care. The **Quality Compliance Specialist** will provide quality compliance support...to ensure that the development, manufacture and distribution of medical products are in compliance with company… more
- Montage Marketing Group (Rockville, MD)
- …you have a strong background in developing and executing security and compliance strategies for federal government contracting organizations? Are you a natural ... for an IT Manager - Systems Administration, Security, and Compliance to join our growing team. Qualified candidates will...aspects of the office network, devices, Bring Your Own Device program, ZOOM Phones ensuring that all devices and… more
- Danaher Corporation (Chaska, MN)
- …medium/large design changes and technology transfer projects in the Medical Device or Diagnostics regulatory environment, ensuring compliance with ISO 13485 ... pay. We offer comprehensive package of benefits including paid time off, medical /dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay… more
- Stryker (Mahwah, NJ)
- …+ Thorough knowledge and understanding of US and international medical device regulations. **Preferred** + Experience in compliance risk situations. + Strong ... HQ, and cross-functional teams. **What you will do** + Ensure QMS compliance with internal and external regulatory requirements (FDA, ISO, MDD, country-specific). +… more
- Danaher Corporation (Minneapolis, MN)
- …include: + Bachelor's degree with 6+ years clinical quality experience within diagnostics or medical device industry, or Master's or Doctoral degree with 4 years ... understanding of ISO 14155, 13485, 14971, 20916, in vitro diagnostic regulation (IVDR), medical device regulation (MDR), and pertinent sections of 21 CFR. +… more
- GE HealthCare (Waukesha, WI)
- …and sustaining engineering; Lead system verification and validation planning and execution; Ensure compliance with medical device regulations (eg, FDA, IEC ... innovative and high-quality imaging solutions. GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a… more
- US Tech Solutions (South San Francisco, CA)
- …new eQMS software to support digital health application and medical device product development. + Individual will ensure compliance with industry regulations ... cross-functional teams. + General experience with user acceptance testing in medical device /pharmaceutical environments **.** **Education:** + Associate or… more
- Teleflex (Wayne, PA)
- …audit, or a related regulatory field preferred. * Experience in the medical device , pharmaceutical, or broader healthcare industry is strongly preferred. ... Global Compliance Analyst **Date:** Oct 3, 2025 **Location:** Wayne,...:12570 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to… more
- J&J Family of Companies (Raritan, NJ)
- …Experience: Either combined or separately, 20+ years of experience in Pharmaceutical or Medical Device Quality Assurance or Quality Operation and/or Regulatory ... for humanity. Learn more at https://www.jnj.com **Job Function:** Legal & Compliance **Job Sub** **Function:** Enterprise Compliance **Job Category:** People… more