Posted:3 hours ago|
Platform:
Work from Office
Full Time
Roles and Responsibilities Ensure compliance with cGMP guidelines during documentation review, approvals, and vendor qualification. Conduct artwork checking, document preparation, FDCA applications, OOS investigations, and factory coordination. Review documents such as BMR/BPR/SOPs/protocols for quality control purposes. Coordinate with cross-functional teams to ensure smooth operations. Desired Candidate Profile 2-5 years of experience in a similar role within the pharmaceutical industry. Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Science (MS/M.Sc). Strong understanding of Good Manufacturing Practices (cGMP), Document Management Systems (DMS), Quality Control procedures.
Vega Biotec
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