- Actalent (Irvine, CA)
- Design Assurance Quality Engineer Job Summary This position is responsible for supporting electrode product and process sustaining activities through the application ... of Quality engineering skills for medical devices. Focuses on process,...of EN ISO 13485, ISO 14971, IEC 62304 and FDA QSR for Medical Devices + Ability to work… more
- BD (Becton, Dickinson and Company) (Brea, CA)
- **Job Description Summary** The Director, Quality Engineering - WW IPD is responsible for developing and leading the global Design Center Quality function for ... expectations for safety and effectiveness. Reporting to the VP, Quality Management WW IPD & MDS Manufacturing EMEA, the...staff. * Deep knowledge of global medical device regulations ( FDA , EU MDR, etc.). * ASQ certification (Engineer or… more
- Gilead Sciences, Inc. (La Verne, CA)
- …in SAP or similar ERP systems for supplier master data + Exposure to FDA inspections, mock audits, and quality systems assessments + Strong interpersonal and ... are seeking a highly motivated **Senior Manager** to join the **Global Supplier Quality ** team within External Quality Operations. This position will support… more
- Takeda Pharmaceuticals (Los Angeles, CA)
- …**About the role** This position holds ultimate responsibility for the overall Quality Assurance of Site Teardown and Fractionation Operations at Takeda's Los ... Manufacturing Facility. The role is essential in ensuring that all quality -related activities meet regulatory standards and uphold Takeda's commitment to excellence.… more
- Cordis (Irvine, CA)
- …that address unmet and critical medical needs. **Responsibilities** The **Senior Engineer, Quality Manufacturing** , joining the Quality team, will be ... responsible for ensuring that our medical devices meet the highest quality standards throughout the manufacturing process. You will be responsible for supporting and… more
- Kelly Services (Anaheim, CA)
- **Director of Quality and Regulatory Affairs** Kelly(R) Science & Clinical is seeking a **Director of Quality and Regulatory Affairs** for a **direct-hire** ... role, you will be responsible for developing, coordinating, and implementing quality and regulatory strategies and programs required for the development, regulatory… more
- J&J Family of Companies (Santa Clara, CA)
- …more at https://www.jnj.com/medtech Johnson & Johnson is recruiting for a **Staff Software Quality Engineer** , located in Santa Clara, CA. Our team advances the ... MONARCH (TM) surgical robotics platform by providing quality engineering support and leadership for design of new...and analytical skills + Working knowledge of IEC 62304, FDA 's General Principles of Software validation, ISO 13485, ISO… more
- Danaher Corporation (Brea, CA)
- …which makes everything possible. The Global Supplier Quality Engineer - Systems and Innovation for Beckman ... responsible for l eading the development of best-in-class supplier quality processes, tools, and system s, with emphasis on...plus if you also possess : + Experience in FDA -regulated or medical device manufacturing environments. + Familiarity with… more
- Danaher Corporation (Brea, CA)
- …which makes everything possible. The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics ... will serve as a critical quality liaison between Beckman Coulter and our key electronics...plus if you also possess : + Experience in FDA -regulated or medical device manufacturing environments. + Certifications such… more
- AbbVie (Irvine, CA)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Quality Systems Senior Specialist is responsible for providing quality ... will ensure that all product, process or system related quality activities from raw material inspection through shipment of...required to prepare and present data during regulatory audits ( FDA , EMA, Anvisa, etc) and internal audits. *Interact with… more