The Surgical Regulatory Affairs Manager handles all regulatory development aspects for surgical devices as assigned. These include IOLs, Inserters and Solutions. The incumbent participates on the product development team to provide regulatory guidance for surgical devices assigned. They also manage relevant regulatory strategy components and interactions with Regulatory Authorities for their assigned surgical products and may perform due diligence efforts on new product opportunities.
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2013…..NOW HIRING….GMP QA Associate…..Ardea Biosciences/Astra Zeneca
Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking an Associate Director, Analytical Sciences to join its’ dynamic team.
The successful candidate will assure cGMP compliance with applicable regulatory requirements including audits and ...
Ardea Biosciences/Astra Zeneca…NOW HIRING...Sr. CRA/CRA, San Diego, CA
Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases.
Ardea is searching for a Sr. Clinical Research Associate/Clinical Research Associate to join the team.
Job Summary
The Senior Clinical Research Associate (Sr. CRA)/Clinical Research Associate (CRA) will ...
Responsible for providing comprehensive Records Management and Documentation support and guidance to departments requiring Records Storage and/or QA Controlled Documentation support. Ensures that Oceanside documentation consistently meets our customer and regulatory requirements.
Job Responsibilities:
- Responsible for performing, monitoring and maintaining tasks and responsibilities for Oceanside Records Management and serve as single point of contact.
- Monitor QA Documentation Vaults in ...
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