Public affairs specialist jobs in Aliso Viejo, CA

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

Title. Regulatory Affairs Specialist. Contractor Pay Rate. 58.79 hr (W 2) Job Description. Compile and maintain regulatory documentation databases or systems. Coordinate efforts associated with..

This role is on site. Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to.. collaborate with Product Regulatory and Regional Regulatory Affairs colleagues to drive timely and..

A medical device client of ours in the East Bay Area is looking to bring on a Regulatory Affairs Specialist IV position! MUST BE ABLE TO COMMUTE TO EAST BAY AREA 3 DAYS A WEEK ON SITE (2 DAYS..

Pay Range. 48. 50 per hr. Depending on experience level Purpose. Completes and maintains regulatory approvals and clearances of medical device products. Key Responsibilities. 1. Re..

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..

Roth Staffing is looking for a Seniro Regulatory Affairs Specialist for our client in Irvine, CA. This is an exciting opportunity to work for a global leader in life saving medical devices with..

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..

B. is highly preferred. li. li Strong technical writing and documentation skills. li. ul. li. li. p. b Education. b. Bachelor&apos s degree in a related field (e.g., Regulatory Affairs..

Biology, biochemistry, medical technology or similar. years of experience in Reg Affairs, QA, R&D.. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs..

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..

This position is responsible for assisting in obtaining regulatory approvals and ensuring compliance to FDA and international regulatory agency requirements including ISO, local, s..

Summary Seeking a Senior Regulatory Affairs Specialist with expertise in US and EU regulatory.. years of experience in regulatory affairs, specifically in the medical device industry.In depth..

Job Description. Pay Range. 44.60hr. 49.60hr. Responsibilities. Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submissi..

Prin Regulatory Affairs SpecialistW2 OnlyContract RolePrincipal RA Specialist will play a key role in.. Minimum of 7 years of experience medical device regulatory affairs Or advanced degree with a minimum of..

Excellent communication skills Purpose Statement. The Regulatory Affairs Specialist supports the.. With supervision, the specialist reviews, plans and prepares regulatory documents and labelling for..

Position Requirements Minimum two years of experience in Regulatory Affairs or Quality Assurance in the medical device industryMinimum one year of active experience applying design..

Job Description Position. Sr Regulatory Affairs SpecialistLocation. Sunnyvale, CaliforniaPosition Type.. Contract Date. 02 21 2023Salary. Starting at. 50.00 The Sr Regulatory Affairs Specialist is responsible..

Minimum five (5) years of experience in Regulatory Affairs.Knowledge and Abilities Proficient knowledge.. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice..