Regulatory affairs manager jobs in Garden Grove, CA

A company is looking for a Regulatory Affairs Manager to oversee regulatory initiatives for implant and.. Key Responsibilities. Develop and implement regulatory strategies for global medical device clearances..

Title. Senior Manager, CMC Regulatory Affairs, Biologics. Location. Foster City, CA. Remote. Contract.. Extensive interaction with departments outside of CMC Regulatory Affairs to define strategy and..

Description The Senior Manager in Regulatory Affairs is responsible for developing and managing.. FDA and global regulatory bodies. This role involves providing direct support for regulatory submissions..

Regulatory Affairs Manager. Permanent. Remote Proclinical is seeking a Manager, Regulatory Affairs for a.. This role is a global regulatory position, working closely with site Quality, R&D, Operations, and..

Position Summary. Reporting to the Senior Director of Regulatory Affairs, the Manager Senior Manager.. This position is onsite. Key Responsibilities. Actively participate as a member of the Regulatory..

Regulatory Affairs Director required by Barrington James for an initial 12 month, remote contract opportunity with the client based in South San Francisco. This contract will be about 30 hours a..

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..

Purpose Statement. The Regulatory Affairs Specialist supports the development and implementation of the.. With supervision, the specialist reviews, plans and prepares regulatory documents and labelling for..

Job Description. Regulatory Affairs Specialist. On site 5x a week in Alameda, CA Must be able to work on.. Regulatory Affairs Specialist Employment Type. Contract Years Experience. 2 5 years of regulatory..

hr including individual healthcare coverage Position Summary. The Regulatory Affairs Specialist.. With supervision, the specialist reviews, plans and prepares regulatory documents and labelling for..

Job Description. Pay Range. 44.60hr. 49.60hr. Responsibilities. Create regulatory submissions.. track timelines and document milestone achievements, participate in developing regulatory strategy..

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..

R&D Partners is seeking to hire a Senior Manager, Regulatory Affairs III in Foster City, CA.Your main.. Extensive interaction with departments outside of CMC Regulatory Affairs to define strategy and..

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..

Role Executive Director Senior Director of Regulatory Affairs Bay Area. Hybrid Company Description This.. Role Description This role leads global regulatory efforts to help develop and manage innovative..

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.. LOCAL APPLICANTS ONLY Requirements. 8. Years of Regulatory Affairs experience across the medical device..

They are looking to bring on a Senior Director, Regulatory Affairs to the team. Key Responsibilities.. Lead and mentor a high performing regulatory team, focusing on staff development and succession planning..

A leading provider in the health care and digital health space is seeking a Senior Regulatory Affairs.. Minimum of 5 years of experience in medical device Regulatory Affairs with a deep understanding of..

Associate Director, Clinical Regulatory Affairs Position Fast Facts and Must Haves. Team is looking for.. Applicants should have a breadth of clinical regulatory experience and have the ability to do strategy..