Officer, QA Doc Cell
Core
Supports the quality assurance documentation cell in pharmaceutical manufacturing by defining quality activities, maintaining documentation infrastructure, and ensuring compliance with regulatory standards.
Role type
Quality Assurance Documentation Specialist
Builds
Quality documentation systems and processes for pharmaceutical products
Domain
Pharmaceutical manufacturing / Regulatory compliance
Deliverable
dashboards & analysis
Required skills
cGMP compliance, 21 CFR Part 210/211 knowledge, deviation management, change control, audit participation, APQR reporting, vendor quality interaction
Preferred skills
B. Pharm or M. Pharm degree, 1+ years of experience in QA documentation
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