- Kelly Services (Sacramento, CA)
- …your career, join us as we pioneer progress in the biotechnology and medical device industries. **Workplace:** Onsite in Sacramento, CA. **Position Title:** ... standards. You will ensure compliance with cGMP, GLP, and regulatory benchmarks, protect product quality , and champion...at $25.0 per hour. + Annual bonus eligibility. + Medical , dental, vision coverage, paid time off, and 401k… more
- Danaher Corporation (Sunnyvale, CA)
- …Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) ... Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Quality Systems Specialist III is responsible for functioning as… more
- Abbott (Milpitas, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... or SysML), is highly desirable + Detailed experience with medical device development processes and FDA 510K...device development processes and FDA 510K and PMA regulatory requirement **Preferred Qualifications** + Good knowledge of and… more
- Actalent (Vista, CA)
- …require. Essential Skills + ISO auditing + Quality Management System (QMS) + Quality assurance + Medical device auditing + CAPA (Corrective and ... The QA Specialist is primarily responsible for overseeing the quality and regulatory aspects of the company....etc. to FDA authorities. + File Vigilance Reports or Medical Device Reports to Competent Authority or… more
- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... from concept to clinical study report per timelines and quality standards. **This role is located in Alameda, California.**...California.** **What you'll do:** + Conduct single or multi-center medical device clinical studies. + Perform study… more
- Herbalife (Lake Forest, CA)
- …+ Knowledge of basic cGMP and QA/QC regulations for the food, pharmaceutical or medical device industry. + Familiarity with safe work practices to include proper ... Technician I, Quality Assurance - 2nd Shift Category: Quality...and SOPs + Collect samples for submission to state regulatory agency. + Sample and perform inspections of components… more
- Terumo Neuro (Aliso Viejo, CA)
- …Description:** Responsible for leading robust manufacturing process development and enhancement in medical devices for both existing and new product development, ... the design, development, and optimization of manufacturing processes for new or existing medical devices . + Apply methodologies like Design of Experiments (DOE)… more
- Praxair, Inc - a Linde Company (Fresno, CA)
- …Quality incidents are properly reported, documented and investigated and manage Quality relationships with suppliers and regulatory authorities. The ... procedures to meet and exceed government compliance requirements for medical gases and other quality assurance requirements....experience) What you will be doing: + Provide FDA regulatory and Quality systems support to assigned… more
- J&J Family of Companies (Irvine, CA)
- …years of quality , manufacturing, or research and development experience in a medical device or other regulated industry + Ability to define problems, collect ... https://www.jnj.com **Job Function:** Supply Chain Engineering **Job Sub** **Function:** Quality Engineering **Job Category:** Scientific/Technology **All Job Posting Locations:**… more
- J&J Family of Companies (Irvine, CA)
- …years of quality , manufacturing, or research and development experience in a medical device or other regulated industry + Ability to define problems, collect ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Quality Assurance **Job Category:**… more