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Job description

Roles and Responsibilities • Ensure compliance with cGMP regulations and company policies during BMR reviews. • Implement change controls by reviewing CAPAs, conducting audits, and ensuring timely closure. • Prepare for OSD inspections by gathering relevant documents and providing training to team members. • Collaborate with cross-functional teams to resolve quality issues and improve processes. • Conduct BPR review meetings, including preparation of agendas, minutes, and follow-up on action items. Desired Candidate Profile • Strong understanding of BPR review, Change Control, Cleaning Validation, Equipment Qualification, GMPs/cGMPs principles. • 3-8 years of experience in IPQA or related field (B.Pharma + M.Pharma). • Excellent communication skills for effective collaboration with stakeholders. • Ability to work independently with minimal supervision while maintaining high standards of accuracy.

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