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A Pharmaceutical client is looking for a Senior Quality Assurance Specialist , specifically with documentation experience in biotechnology or pharmaceutical industry
Job Overview
Senior QA Documentation Specialist, you will be instrumental in the management and evolution of the Veeva Learning Management System to meet the challenges of compliance in late-stage clinical drug product and commercial drug product. The Senior QA Documentation Specialist will be responsible for supporting the daily activities of Documentation Management.
Job Functions : (Primary essential duties and responsibilities)
Required Knowledge, Skills and Abilities:
· Experience with Veeva Quality Vault: QualityDocs
· Strong working knowledge of cGxPs and international regulatory requirements
Full Time
$88k-106k (estimate)
06/25/2024
07/08/2024
thriveps.org
SAN DIEGO, CA
25 - 50
Private
<$5M
Elementary & Secondary Education
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