- BD (Becton, Dickinson and Company) (San Diego, CA)
- …of five (5) years of Regulatory Affairs experience in the medical device industry required + Strong prioritizing, interpersonal, communication, and ... new and existing US and international regulations and directives (eg, FDA Medical Device Regulations, EU Low Voltage Directive, EU Electromagnetic Compatibility… more
- Abbott (Alameda, CA)
- … medical device regulations and submissions. . Familiar with relevant regulatory requirements for medical devices including Quality Systems standards, ... Qualifications . 5 years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a… more
- J&J Family of Companies (Santa Clara, CA)
- … fields is preferred + 0 - 1 years' experience in medical device , life science, pharma industry Experience in regulatory affairs is preferred + Highly ... Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated… more
- Gilead Sciences, Inc. (Foster City, CA)
- …to accelerate development and approval timelines. Provide guidance to PDM Teams and Device Teams to align development and regulatory path for combination ... Description** . **Strategic Leadership & Vision** Define and drive global regulatory strategies for combination products, ensuring alignment with corporate goals and… more
- Kelly Services (Irvine, CA)
- …least 5 years of experience in a Quality , Manufacturing or Engineering function in medical device industry * At least 5 years of experience in a Quality ... ** REGULATORY COMPLIANCE - SENIOR ANALYST (Hybrid)** QUALIFICATIONS: a)..., Manufacturing or Engineering function in medical device industry * Experience with MDSAP Audits, health authorities… more
- Abbott (Sylmar, CA)
- …(eg, medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support, ... regulatory professionals **Premarket:** + Assess the acceptability of quality , preclinical and clinical documentation for submission filing + Compile, prepare,… more
- Kelly Services (South San Francisco, CA)
- …member of the global RA department. + Seeks expert advice and develops device regulatory product strategies and identifies data and information requirements as ... also offers the opportunity to work alongside the IVD Quality team in the development and implementation of processes...related life sciences + Required Experience: 5+ years of regulatory experience in IVD, companion diagnostics, medical … more
- Abbott (Santa Clara, CA)
- …Multitasks, prioritizes and meets deadlines in a timely manner. + Experience working in the Medical Device industry. + Certification is a plus (such as RAC from ... regulatory compliance. **Premarket:** + Assess the acceptability of quality , preclinical and clinical documentation for submission filing. + Compile, prepare,… more
- Kelly Services (Petaluma, CA)
- …$80-$90/hr **About the Opportunity** Kelly Engineering is partnering with a fast-growing medical device and pharmaceutical company that is preparing for multiple ... Engineering Specialist** who can bridge the gap between engineering, quality , and regulatory functions. This role is...related field (advanced degree preferred). + 5+ years of regulatory or compliance experience in medical devices,… more
- Abbott (Santa Clara, CA)
- …Multitasks, prioritizes and meets deadlines in a timely manner. + Experience working in the Medical Device industry. + Certification is a plus (such as RAC from ... regulatory compliance. **Premarket:** + Assess the acceptability of quality , preclinical and clinical documentation for submission filing. + Compile, prepare,… more