Regulatory specialist jobs in Tustin, CA

Regulatory Affairs Specialist II Location. Irvine, CA (Hybrid 3 days on site) 12 month Assignment Pay.. 5. 49 hr. On behalf of our client a medical device client, we are seeking a Regulatory Affair's..

Position Title. Regulatory Affairs Specialist Length of Contract. 12 months (Potential Extension.. Irvine. Hybrid Purpose Statement. The Regulatory Affairs Specialist supports the development and..

Regulatory Affairs Associate 6 month contract Onsite in Alameda, CA Responsibilities. Responsible for filing necessary applications and handling all government interactions pertain..

R&D to join our growing team. The Regulatory Specialist is a part of Research and Development, this team.. RESPONSIBILITIES Oversee day to day regulatory operations (formula review, filings, formula testing..

Job Title. Senior Regulatory Affairs Specialist Location. San Diego, CA Experience. Must have experience.. The Sr. Regulatory Affairs Specialist will coordinate the collection of technical information and..

Overview Co ordinates and prepares document packages for regulatory submissions from all areas of the.. Keeps abreast of regulatory procedures and changes. May interact with regulatory agencies. Works on..

Pay Range. 48. 50 per hr. Depending on experience level Purpose. Completes and maintains regulatory.. Key Responsibilities. 1. Represent the regulatory function on manufacturing and product development..

Roth Staffing is looking for a Seniro Regulatory Affairs Specialist for our client in Irvine, CA.. Job Descirption. Purpose. Completes and maintains regulatory approvals and clearances of medical device..

This On site role reports directly to the CEO. The Senior Regulatory Specialist is responsible to plan.. collaborate with Product Regulatory and Regional Regulatory Affairs colleagues to drive timely and..

Job Description Job Description Job Summary. Responsible for managing submission publishing, device listings, UDI data collection, and maintaining regulatory compliance for medical devices in..

Program and Regulatory Specialist (Electric Generation System Program Specialist I) Salary. 9,832.00.. The Energy Commission seeks a Program and Regulatory Specialist to fill one position in the Special..

Full Time, Onsite Overview. A leading provider in the health care and digital health space is seeking a Senior Regulatory Affairs Specialist to join their regulatory team. The company focuses on..

Assess the appropriate regulatory reporting mechanism using FDA regulations, guidance documents, and in.. Work closely with Regulatory Affairs, Quality Assurance, Marketing, and Product Development teams to..

R&D Partners is seeking to hire a Regulatory Affairs Specialist II in Lake Forest, CA.Your main responsibilities as a Regulatory Affairs Specialist II Compile and maintain regulatory..

Support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact all Bio Rad products currenlty CE Marked under the IVD Directive. Activites include pr..

From design to production, our Regulatory Affairs teams help guide our innovative technologies through.. Join us and be part of our inspiring journey.How you will make an impact As a Specialist, Regulatory..

Regulatory Affairs Specialist Brett Fisher Group. Irvine, CA, United States Why Join?Our client is a.. The role of the Regulatory Affairs Specialist will be to support the global regulatory affairs of the..

Preferred Education and Experience. 10. years of legal practice in healthcare regulatory and.. Preferred Education and Experience. 10. years of legal practice in healthcare regulatory and..

Job Description Job Description In Vitro Diagnostic Regulatory Specialist (R&D QA) Irvine, CA 92618 ( Local candidates. 3 days on site 2 days remote). 40. 45hr (Weekly pay. Benefits) 1yr..