- Abbott (Temecula, CA)
- …problem solving and project management skills. + Experience in manufacturing engineering experience, medical device experience required. + International ... **_MAIN PURPOSE OF ROLE_** This role will provides technical and sustaining engineering support in a manufacturing area. Recommends and implements equipment… more
- Abbott (Menlo Park, CA)
- …10%, including internationally. + Proficient in CAD **Preferred Qualifications** + Prior manufacturing / Medical device engineering experience + Preferred ... equivalent combination of education and work experience. + Minimum 5 years manufacturing engineering experience + Strong analytical, problem solving and project… more
- Kelly Services (Irvine, CA)
- …performance: * At 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, Manufacturing or Engineering function in medical device industry * Experience with MDSAP Audits, health authorities and notified… more
- Gilead Sciences, Inc. (Foster City, CA)
- …action. + Experience in the pharmaceutical or biotechnology industry is preferred + Medical device or combination product experience is preferred + PMP ... goals, and results to team members across functions and departments, including device development, packaging, quality, regulatory affairs and manufacturing . +… more
- Mallinckrodt Pharmaceuticals (Sacramento, CA)
- …or a related field, or equivalent military experience + 4+ years of experience in medical device cGMP service, manufacturing , or a comparable combination of ... Job Title Senior Technical Product Specialist - Medical Device Requisition JR000015165 Senior Technical Product Specialist - Medical Device (Open)… more
- US Tech Solutions (San Bruno, CA)
- …system issues. **Mandatory:** + 5+ years of experience in program management. + Experience in Medical Device Manufacturing or Software as a Medical ... **Responsibilities:** + Managing cross-functional or cross-team projects to bring regulated medical device products to market. + Ensuring product specifications… more
- AbbVie (Irvine, CA)
- …CFR Parts 3, 4, GCP, GLP, 210/211, 820 QSR (Design Control), European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP, technical standards, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...regulations and company policies and procedures. Analyzes and approves manufacturing change requests. + Represents RA Device … more
- Adecco US, Inc. (Santa Clarita, CA)
- …our clients in Valencia with a Medical Device QC Inspector for a medical device manufacturing company. This is a temporary opportunity for the right ... Medical Device QC Inspector Adecco is... Medical Device QC Inspector Adecco is currently assisting one...about the position, please Apply Now! Responsibilities: + Interprets engineering drawings and schematic diagrams. + Assist with the… more
- AbbVie (Pleasanton, CA)
- …Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 ... (QSR), ISO 13485, ISO 14971, MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes & GMP; & +… more
- Cordis (Irvine, CA)
- …address unmet and critical medical needs. **Responsibilities** The Manager of Manufacturing Engineering will plan, direct, and coordinate activities for the ... the prescribed time frame and funding parameters of the manufacturing engineering group by performing the following...equivalent work experience + 5+ years' experience in the medical device /pharmaceutical field or in a related… more