- J&J Family of Companies (Irvine, CA)
- …study team; + Cooperates with cross-functional teams (Research & Development, Complaint Handling, Quality / Regulatory , Medical Affairs, Medical Safety) to ... + Cooperation with the necessary stakeholders (clinical study team, medical , clinical sites, regulatory , data management) on...+ Clinical/ medical background is a plus. + Medical device experience is highly preferred. +… more
- Kelly Services (Santa Clara, CA)
- …Training Specialist** . This is a temp-hire contract with one of our Global Medical Device Robotics & Digital Solutions clients, located in **Santa Clara, CA.** ... this group you will be eligible for 50% paid Medical & Dental, a 401K plan, and a variety...Coordinates the performance of audits to assess compliance with quality and regulatory requirements. Demonstrates Leadership Imperatives… more
- AbbVie (Irvine, CA)
- …compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- AbbVie (Pleasanton, CA)
- …compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- US Tech Solutions (San Bruno, CA)
- …for medical devices , specifically focusing on Software as a Medical Device (SClient) or low-risk enforcement discretion products. 2. At least 3-5 ... Regulatory Compliance:** 1. Ensure compliance with US FDA Quality System Regulations, ISO 13485, and integration of best...ISO 13485, and integration of best practices from the medical device industry. **Documentation and Support:** 1.… more
- Abbott (Alameda, CA)
- …+ Must have 5+ experience in Software Quality Assurance. + Knowledge of medical device standards including FDA QSR, ISO 13485, ISO 14971, 21 CFR Part ... File (DHF) and Device Master Record (DMR) are in compliance with regulatory standards and quality management policies and procedures. + Develops and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …goals, and results to team members across functions and departments, including device development, packaging, quality , regulatory affairs and manufacturing. ... + Experience in the pharmaceutical or biotechnology industry is preferred + Medical device or combination product experience is preferred + PMP certification is… more
- Abbott (Alameda, CA)
- … quality -related field. + 5+ years of experience in quality assurance or regulatory compliance in the medical device industry. + Strong knowledge of ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Danaher Corporation (West Sacramento, CA)
- …Microbiology Team via PPG, and functional leaders. + Drive achievement of Quality , Cost, and Delivery (QCD) metrics. + Identify risks and implement countermeasures ... 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
- Gilead Sciences, Inc. (La Verne, CA)
- …guard issue resolution, auto-injector issues, component manufacturing) + Understanding of Quality Management Systems and regulatory requirements + Experience ... are seeking a highly motivated **Senior Manager** to join the **Global Supplier Quality ** team within External Quality Operations. This position will support… more