- CTG (Woodland, CA)
- …preferred) **Qualifications** * Minimum 3 years' experience in Quality or Regulatory , preferably in medical device , pharmaceutical, or biotechnology ... Quality Engineer II will develop and support all Quality Management System (QMS) and Regulatory Affairs (RA) activities in alignment with site quality … more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …technical field + Minimum of 10 years of experience in Quality or Regulatory function within the medical device industry, including experience with Class ... Collaborates with leadership in Business Unit Quality , Regulatory Affairs, R&D, Operations, Service, Medical Affairs,... Quality Operations, etc.) + Experience in full Medical Device product lifecycle. Ie Demonstrated … more
- J&J Family of Companies (Irvine, CA)
- …study team; o Cooperates with cross-functional teams (Research & Development, Complaint Handling, Quality / Regulatory , Medical Affairs, Medical Safety) to ... R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and.... Clinical/ medical background is a plus. . Medical device experience is highly preferred. REQUIRED… more
- US Tech Solutions (San Bruno, CA)
- …align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process Verification, ... (eg, Statistical Analysis, NC/CAPA, Audits) and US and International Medical Device Regulations & Regulatory ...and regulatory submissions. + Support bringing novel medical devices from concept to release, manage… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Provide guidance to PDM Teams and Device Teams to align development and regulatory path for combination products and devices . . **Global Regulatory ... global CMC regulatory initiatives focused on combination products and devices . Ensure regulatory conformance and consistency across markets, maintaining… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- … bodies. + Understanding of regulations, standards and guidelines related to IVD, and/or medical devices and quality systems including 21 CFR, CE-IVD, ISO ... these activities. By working successfully across functions-including Program Management, Marketing, Regulatory , Quality , and Medical Affairs-this leader will… more
- Aerotek (Irvine, CA)
- **HIRING 1st Shift Medical Device Assembler** Job Description We are seeking a dedicated Assembler I to join our team on a 12-18 month contract. This role ... involves assembling and testing medical devices using a variety of tools,...processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +… more
- Aerotek (Irvine, CA)
- **HIRING 2ND SHIFT - MEDICAL DEVICE ASSEMBLER** Join a dynamic team as a 2nd Shift Assembler, where you will play a crucial role in the assembly and testing of ... medical devices . This position requires flexibility with...processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +… more
- Aerotek (Irvine, CA)
- ** Medical Device Assembler I - 1st Shift** **Job Description** We are seeking a dedicated Assembler I who will be responsible for assembling and testing ... medical devices using a variety of tools,...processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +… more
- Aerotek (Irvine, CA)
- **Job Title: 2nd Shift Medical Device Assembler** **Job Description** Join a dynamic team as a 2nd Shift Assembler where you'll play a crucial role in the ... assembly and testing of medical devices . This position offers an opportunity...processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +… more