- Astrix Technology (Irvine, CA)
- ** Quality Specialist ( Medical Device )** Quality Control Irvine, CA, US Pay Rate Low: 32.00 | Pay Rate High: 36.00 + Added - 26/08/2025 Apply for Job ... Exciting Quality Engineer Specialist development opportunity to work for a...regulations (21 CFR 820/803), ISO 13485 + Experience with medical device complaint handling and regulatory… 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 ... Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management… 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 ... processes, and procedures. + Comply with policies, guidelines, and regulatory requirements per the Quality System. +...the shift. **Additional Skills & Qualifications** + Experience in medical device assembly. + Cleanroom experience is… 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 ... School Diploma or equivalent. + Familiarity with cleanroom environments is beneficial. + Medical device assembly experience is preferred. **Why Work Here?** Be… 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
- Actalent (San Diego, CA)
- …of new and revised labeling materials. Required Skills & Experience: + Experience in medical device labeling and regulatory compliance. + Proficiency in ... the labeling process for both new and existing In Vitro Diagnostic (IVD) and Medical Device (MD) products. This role requires cross-functional coordination and a… 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
- AbbVie (Irvine, CA)
- …compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to… 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...work collaboratively with a team to design and develop medical products from initial concept through the transfer to… 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