CAREERS
CAREERS
| Senior QA Associate, Document Control and Management | Details | Submit Resume |
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Bedminster, NJ Responsible for implementation and maintenance of Electronic Document Management System SOPs to reflect current practices. Establish and maintain CGMP compliant document management procedures to include SOPs, vendor qualification, document and change control, deviations, investigations, CAPAs, annual product reviews, and audits. Manage coordination of internal and external review, approvals and controls of document s related to Quality Systems and CGMP compliance procedures. Candidates should have Bachelor's degree with 3+ years of document control and management experience with Quality Assurance functions in the pharmaceutical industry. |
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