- Meta (Menlo Park, CA)
- …an experienced attorney to serve as Associate General Counsel for Healthcare and Medical Device Compliance on Facebook's Corporate Compliance & ... in an exciting, dynamic environment. **Required Skills:** Healthcare and Medical Device Compliance Responsibilities: 1. Oversee a high-talent team in… more
- IQVIA (Palo Alto, CA)
- …Sales Consultants_** to join our team of field employee's. **Associate Sales Consultant - Medical Device ** If you have ever wondered about the intricacies of ... surgical procedures or considered a career path in medical device sales, this is the role...and maintain the highest levels of professionalism, ethics and compliance at all times. + Analyze product performance and… more
- Wells Fargo (San Francisco, CA)
- …and commercialization. The team focuses its efforts on subsectors such as Biotech/Pharma, Medical Device , Digital Health, Healthcare IT, Pharma Outsourcing, ... **About this role:** The Emerging Healthcare Technologies (EHT) group within Wells Fargo's ...customer relationships balanced with a strong risk mitigating and compliance -driven culture which firmly establishes those disciplines as critical… more
- Abbott (Pleasanton, CA)
- …**The Opportunity** This position works out of our **Pleasanton, CA** location in the Medical Device division. Our medical devices help more than 10,000 ... Compliance Management or related experience + 5 years in Medical Device /Pharma Industry **Preferred Qualifications** + Strong understanding of ISO/MDSAP… more
- GRAIL (Menlo Park, CA)
- …counsel. + 20+ years of Compliance and Privacy experience in in-house medical device , biotech, clinical laboratory, pharmaceutical, or other life sciences or ... & HCOs: provide strategic counseling guidance across Commercial and Medical on interactions with HCPs & HCOs, including procedures,... issues and related policies and procedures. + Global Healthcare Compliance : update GRAIL policies to address… more
- Abbott (Pleasanton, CA)
- …field + Eight (8) years of Quality Systems, Quality Assurance and/or Regulatory Compliance /Affairs experience in medical device manufacturing or other ... healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...get on with their lives. As a Senior Quality Compliance Manager, the individual will play a crucial role… more
- Philips (Fremont, CA)
- …You've acquired a minimum of 12+ years' experience in global, FDA regulated medical device environments, including proven functional and strategic leadership of ... The Director of Quality & Compliance plays an important leadership role within Philips'...regulated QMS. + You have proven expertise/knowledge of global medical device regulations, requirements, and standards, such… more
- Abbott (Alameda, CA)
- …focused manufacturing environment. * Working knowledge of regulations and standards affecting Medical Device manufacturing (eg QSR, ISO, EN Quality System ... of healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve… more
- Abbott (Alameda, CA)
- …for the Medical Events Group as required. + Accountable for meeting the compliance requirements for Medical Device Reporting (803), including but not ... and scientists. The Opportunity Responsible for timely review, documentation and filing of Medical Device Reports to the FDA (US), Medical Problem… more
- Abbott (Alameda, CA)
- … Events Team provides direct supervision and management to staff responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports ... healthcare , with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000... Incident Reports to the EU/EFTA including France, and Medical Device Incident reports to the rest… more
- Abbott (Pleasanton, CA)
- …9+ years' experience in a Quality, Regulatory, or product development role in the medical device industry. + 5+ years' experience managing a team of ... regulations and guidance, ISO 13485, Software Standards (eg, IEC 62304), EU Medical Device Regulations, and MDSAP **Preferred Qualifications** Direct experience… more
- Abbott (Alameda, CA)
- …the rest of world for the division's products. Accountable for meeting the compliance requirements for Medical Device Reporting regulations including (803). ... and scientists. **The Opportunity** Responsible for timely review, documentation and filing of Medical Device Reports to the FDA (US), Medical Problem… more
- US Tech Solutions (San Bruno, CA)
- …Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1. Support the creation ... the way people manage their health and the way healthcare is delivered. The purpose is to bring the...support CAPA, complaints, audits, and overall QMS functions. **Experience:** ** Medical Device Software Experience:** 1. Proven experience… more
- Terumo Medical Corporation (San Francisco, CA)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... broad range of applications for numerous areas of the healthcare industry. TMC places a premium on providing customers...degree and a minimum of 3 years experience in Medical Device Sales with Cath Lab and/or… more
- J&J Family of Companies (Santa Clara, CA)
- …degree in Engineering. + 3-5 years of experience in a medical device environment. + Knowledge of and compliance with applicable Quality System requirements ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease… more
- J&J Family of Companies (Santa Clara, CA)
- …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 ... Johnson is recruiting for Principal R&D Engineer for Shockwave Medical Inc. located in Santa Clara, CA. At Johnson...Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where… more
- Olympus Corporation of the Americas (San Francisco, CA)
- …managing Market Quality- COE MDR team for the regulatory assessment and submission of Medical Device Reports to the FDA and assisting with submissions to other ... MDR Analysts who are responsible for preparing and submitting Medical Device Reports to the FDA for...lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare … more
- J&J Family of Companies (Santa Clara, CA)
- … Medical aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...Minimum of eight (8) years of experience in a medical device environment or equivalent experience in… more
- J&J Family of Companies (Santa Clara, CA)
- … Medical aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...Minimum of five (5) years of experience in a medical device environment or, 3 years of… more
- J&J Family of Companies (Santa Clara, CA)
- …Requirements + Bachelor's Degree Required. + 10+ years of experience in medical device and/or pharmaceutical grant management or equivalent experience. + ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...a Quarterly Global Budget Report to Grant Committee and Compliance . + Collaborate with internal Shockwave Medical … more