- AbbVie (Irvine, CA)
- …marketing plans to deliver strong business performance for AbbVie's only eye care medical device . This person's key responsibilities are to lead the strategic ... process from concept review to final approval, via close collaboration with legal, compliance , regulatory and medical . + Represent the US commercial strategy as… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …ISO 13485. IEC 60601 and IEC 62304 experience a plus. + Experience in medical device and/or regulated industry (required). + Experience with remediation efforts ... Experience:** + 8+ years in a regulated industry, particularly within the medical device , bio-pharmaceutical, or biotechnology sectors, with a strong preference… more
- Abbott (Sylmar, CA)
- …Quality, Compliance , Engineering, within a regulated environment, such as medical device , diagnostics or pharmaceutical industries, to develop the competence ... environment in quality desired. + Industry certification preferred. + Class III or II medical device experience. + 3-5 years in a supervisory/leadership role. +… more
- Edwards Lifesciences (Irvine, CA)
- …including early career professionals seeking to explore and establish themselves within the medical device industry. We'll provide you with the opportunity to ... assignment you will have gained detailed insight into the medical device supply chain. Functional experience may...Sourcing + Logistics + Warehousing + Transportation + Trade Compliance _Specific internship projects will be assigned based on… 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 ... from concept through commercialization. + Design and develop product(s) in compliance with the company's Design Control requirements and consistent with applicable… more
- Actalent (Vista, CA)
- …annual reports, control documents, etc. to FDA authorities. + File Vigilance Reports or Medical Device Reports to Competent Authority or FDA. + Review regulatory ... the Quality System. + Conduct internal audits to ensure compliance . + Receive, review, and respond to customer product...+ Quality Management System (QMS) + Quality assurance + Medical device auditing + CAPA (Corrective and… more
- Fujifilm (Sacramento, CA)
- …and advertising regulations and other regulations specific to Life Sciences/Pharma and Medical Device companies. + Perform other duties as assigned. **Required ... and/or in-house legal department, preferably in the Life Sciences/Pharma, Medical Device or health care field. +...Experience in legal matters involving tariffs and other trade compliance issues would be a plus. + Strong contract… more
- Cardinal Health (Sacramento, CA)
- …future. **Job Summary** The **Account Manager - Sustainable Technologies** covers our medical device reprocessing portfolio. This position, reporting directly to ... Within the Global Medical Products and Distribution ("GMPD") segment, Sustainable Technologies...Sustainable Technologies (TM) is a leading provider of single-use device (SUD) collections, reprocessing, and recycling services in the… more
- Abbott (Alameda, CA)
- …US device regulations, and/ or with EU and other international medical device regulations and submissions. . Familiar with relevant regulatory requirements ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Keeper Security, Inc. (El Dorado Hills, CA)
- …a Technical Product Manager to lead the development of our Privileged Endpoint Device Management (PEDM) solution. This is a 100% remote position with an opportunity ... to prevent breaches, reduce help desk costs and ensure compliance . Trusted by millions of individuals and thousands of...As the Technical Product Manager for Keeper's Privileged Endpoint Device Management (PEDM) solution, you will play a critical… more