- Stryker (Irvine, CA)
- …engineering or related discipline. + 4+ years' related experience required. + Medical device industry experience required. + Familiarity with New Product ... Sigma Green or Black belts are preferred. + Experience with the medical device development lifecycle, including risk management and design/process verification… more
- West Pharmaceutical Services (DE)
- …of quality related experience with preferred experience in pharmaceutical and/or medical device industry + Experience working with suppliers and supplier ... Senior Specialist, Supplier Quality Requisition ID: 71354 Date: Nov 22, 2025...preferred + Knowledge of cGMP, cGDP, relevant ISO standards, medical device requirements and other international regulations… more
- Medtronic (Lafayette, CO)
- …- Provides expertise in interpreting and implementing regulatory requirements, including medical device directives, FDA regulations, and international standards; ... world. **A Day in the Life** As a Sr. Quality Systems Manager, where you'll play a pivotal role...tools (FMEA, FTA, PHA, ISO 14971) + Knowledge of medical device regulations: FDA 21 CFR Part… more
- Roche (South San Francisco, CA)
- …several audit types and leading at least one audit type within GCP and/or Medical Device . + Knowledge of drug development processes and GxP/CS regulations + ... industry and/or industry and/or nonclinical/clinical research + Minimum 2 years in GCP/CS/ Device Quality Assurance role (auditing) Key Competencies + Ability to… more
- AbbVie (North Chicago, IL)
- …global teams. + 15+ years industry experience across pharmaceutical, medical device , combination products, research, development, clinical operations, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...regulatory compliance, and contributes to the overall success of drug/ device development programs. The Sr Director, R&D Quality… more
- Envista Holdings Corporation (Lubbock, TX)
- …Quality position within an FDA regulated industry (ex: tissue banking, medical device , biologics or pharmaceutical industries. **PREFERRED QUALIFICATION:** + ... **Job Description:** **JOB SUMMARY** : The Quality Associate provides quality assurance services...and OpCo standards. **PRIMARY DUTIES & RESPONSIBILITIES:** + Review device batch records for accuracy and compliance to established… more
- Hologic (San Diego, CA)
- …experience in a regulated environment, ideally in the IVD space. + Working knowledge of Quality Management System for Medical Device Manufacturing FDA 21 CFR ... Quality Engineer, Design Control San Diego, CA, United...mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management… more
- Philips (Bothell, WA)
- …Design Quality /Control with extensive experience in both ISO 13485 Medical Device /Technology and ISO 9001, with extensive design/development experience in ... The Director of Design Quality Engineering will play a critical role within...Class I medical device , consumer goods and cosmetics. +...Class I medical device , consumer goods and cosmetics. + You have proven… more
- Mentor Technical Group (Caguas, PR)
- … control, quality assurance, or regulatory compliance, preferably in the medical device or pharmaceutical industry Mentor Technical Group es un empleador ... the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas,… more
- BD (Becton, Dickinson and Company) (Temecula, CA)
- …experience in quality engineering, preferably in a combination product or medical device environment. + Strong knowledge of design control, risk management ... **Job Description Summary** The Lab Services Quality Engineer is responsible for ensuring quality...of possible** BD is one of the largest global medical technology companies in the world. Advancing the world… more