- Owens & Minor (Toano, VA)
- …required. * American Society for Quality (CQA, CQBA, CQE, CQM/OE) and/or Regulatory Affairs Professionals Society or comparable certification preferred. * Or ... and/or other statistical software experience. * Experience in a medical device manufacturing environment preferred. * Medical Device experience, knowledge… more
- Owens & Minor (Morgantown, WV)
- …preferred * American Society for Quality (CQA, CQBA, CQE, CQM/OE) and/or Regulatory Affairs Professionals Society or comparable certification preferred * Any ... Minitab and/or other statistical software experience * Experience in a medical device manufacturing environment preferred * Medical Device experience, knowledge… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …tracking, review, and collection of study-specific documents required in the site's Regulatory Binder. + Assist in tracking study activies and milestones by managing ... and maintaining study tackers and logs. + Manages device accountability for clinical studies, including tracking, shipment, and reconciliation of devices. +… more
- Zimmer Biomet (Englewood, CO)
- …device from ideation to commercialization required. * Understanding of medical device industry regulatory requirements preferred. * Experience with CAD. ... of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a...inspection plans * Aide in publication efforts with Clinical Affairs team * Observe surgery (live, cadaver, or video)… more
- Teleflex (Morrisville, NC)
- …representative during acquisitions, collaborating with teams in Quality Assurance, Regulatory Affairs , Supply Chain, Design, and Manufacturing. Additionally, ... representing supplier quality in cross-functional projects to meet company and regulatory goals. **Principal Responsibilities** * Coordinate with Global … more
- ThermoFisher Scientific (Pittsburgh, PA)
- …**Experience** + Minimum of 3+ years of experience in quality assurance or regulatory affairs , preferably in the pharmaceutical, biotechnology, or medical ... are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our… more
- Envista Holdings Corporation (Brea, CA)
- …whether to accept the product and future purchases from the vendor. + Supports Regulatory Affairs with their activities related to submissions and notified body ... to develop, implement, and maintain quality assurance protocols that comply with regulatory requirements an industry standard. The Sr. Quality Engineer will possess… more
- Lilly (Indianapolis, IN)
- …+ Capable of representing Lilly Gene Therapy professionally with external global opinion leaders, investigators, vendors, regulatory agencies, and others ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
- Kelly Services (Brea, CA)
- …implementation of changes. + Partner with internal teams-including design, planning, regulatory affairs , quality, and marketing-and external suppliers to ... Rate:** $41.34/hour - $50.48/hour **Job Summary** Reporting to the Senior Global Product Manager, the **Associate Product Manager (Temporary)** is responsible for… more
- Cook Medical (Bloomington, IN)
- …with cross function teams including quality, engineering, production, clinical, and regulatory affairs .- Provide leadership in the understanding of medical ... processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements. Must work and interact effectively and professionally with and for others… more