Assistant Manager – QA with 8–10 years of pharmaceutical experience in document control, eDMS management, and retain sample handling. Responsible for leading document issuance activities while ensuring GMP compliance and data integrity. Supports audits, regulatory requirements, and continuous improvement of QA systems.
Industry: Pharmaceutical
Experience: 8–10 Years
Education: B.Sc / M.Sc in Chemistry
Key Responsibilities:
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Handle issuance, control, and archival of quality documents in compliance with GMP and regulatory requirements
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Lead and supervise the Document Issuance Team, ensuring accuracy, compliance, and timely distribution
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Manage and administer eDMS (Electronic Document Management System) including document lifecycle control
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Oversee Reserve/Retain Sample Management,
ensuring proper storage, traceability, and compliance
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Ensure adherence to data integrity, SOPs, and regulatory guidelines
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Coordinate with cross-functional teams during audits and inspections
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Support continuous improvement initiatives related to documentation and QA systems
Desired Skills & Competencies:
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Solid knowledge of GMP, GDP, and regulatory requirements
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Hands-on experience with eDMS software
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Leadership and team-handling capabilities
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Excellent documentation, communication, and organizational skills
Experience Requirement:
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Minimum 8–10 years of experience in Quality Assurance within the pharmaceutical industry