- Abbott (Sylmar, CA)
- …heart arrhythmias, or irregular heartbeats. **The Opportunity** We are presently hiring for a ** Regulatory Affairs Specialist II ** to work on-site at ... industry. + Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Apply Now (https://www.jobs.abbott/us/en) * Participants who… more
- Kelly Services (Irvine, CA)
- ** Regulatory Affairs Specialist ** The Regulatory Affairs Specialist II , will provide administrative and technical support to regulatory ... compliance with US and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide Regulatory support… more
- Abbott (Sylmar, CA)
- …Our location in Sylmar, CA currently has an on-site opportunity for a **Senior Regulatory Affairs Specialist ** with our Cardiac Rhythm Management division. ... contractors, and vendors. + Provides mentoring and leadership to Regulatory Specialist I and II ...attention to detail. **Preferred** **Qualifications** + Master's Degree in Regulatory Affairs and may be used in… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …7. Ability to comprehend technical documents and concepts. **External-Facing Title:** Senior Specialist Regulatory Affairs **Posting Country:** US - United ... **12271BR** **Title:** Sr. Specialist , Regulatory Affairs **Job...writing skills as evidenced by successful US FDA Class II / III medical device submissions, EU CE Mark… more
- Veterans Affairs, Veterans Health Administration (Long Beach, CA)
- …VA Medical Center is currently recruiting for one (1) Medical Technologist, Technical Specialist to work in the Microbiology & Molecular section of Pathology and ... adopts appropriate methods and testing. Applies laws, policies, precedents, regulatory , licensing, and accrediting requirements to establish, monitor, and maintain… more
- Medtronic (Irvine, CA)
- …**Required Knowledge and Experience:** Requires a Baccalaureate degree Minimum of 4 years of regulatory affairs experience or advanced degree with a minimum of 2 ... to Have** + Prior Regulatory Ops experience in medical devices with class II & III products + Experience with EU MDR regulations, including AR verification +… more