- Kelly Services (Irvine, CA)
- …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...CFR Part 820 QSR, ISO 13485, Brazil GMP, Canada Medical Devices Regulations SOR 98-282, Japan's MHLW… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …direct professional experience ( Regulatory ) in increasingly responsible positions in the medical device field and seven (7) years of management experience + ... a **maker of possible** with us. The Sr. Director, Regulatory Affairs is the ranking Regulatory Affairs...science). Advanced degree preferred (Ph.D, MBA) + Experience with Medical devices , pumping systems and/or software driven… more
- Abbott (Alameda, CA)
- …scientific journal of conferences. *Interfaces with key stakeholders on tasks (eg, Regulatory , R&D, Quality , Marketing, Medical Affairs). *Creates/updates ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Kelly Services (Petaluma, CA)
- …preferred). + 5+ years of regulatory or compliance experience in medical devices , pharmaceuticals, or combination products. + Strong working knowledge of ... the Opportunity** Kelly Engineering is partnering with a fast-growing medical device and pharmaceutical company that is...Engineering Specialist** who can bridge the gap between engineering, quality , and regulatory functions. This role is… more
- Cedars-Sinai (Beverly Hills, CA)
- …Los Angeles and beyond. **Req ID** : 11799 **Working Title** : Lead Regulatory Coordinator - Medical Network **Department** : CA Heart Foundation **Business ... Cedars-Sinai Medical Care Foundation **Job Category** : Compliance / Quality **Job Specialty** : Research Compliance **Overtime Status** : EXEMPT **Primary… more
- Abbott (Alameda, CA)
- …+ Work closely with in-country regulatory representatives, compile, prepare, and review medical device or IVD submissions to regulatory agencies in the ... (eg, medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support,… more
- Meta (Sunnyvale, CA)
- …radios & signal emissions, industry certifications, product marking, product safety, and medical devices . Your technical expertise and program management skills ... **Summary:** As a Hardware Regulatory Readiness and Compliance Technical Program Manager at...will be essential in delivering high- quality products that meet customer needs while ensuring compliance… more
- Grifols Shared Services North America, Inc (San Carlos, CA)
- … submissions. + May supervise staff + May have responsibility for maintaining a compliant medical device quality system for R&D and informing project teams ... regulatory strategies for projects and issues affecting development of new products or medical devices or new indications for existing products + Provides … more
- Philips (San Diego, CA)
- …end-users. + You will collaborate with cross-functional stakeholders, including Marketing, Medical Education, Sales, Legal, Regulatory Affairs, and Clinical ... Platform & Process Specialist with the Image Guided Therapy Devices team you will lead the optimization and management...won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work… more
- Abbott (Santa Clara, CA)
- …(eg, medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support, ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more