About the Role:
A prominent pharmaceutical and formulation manufacturer in Boisar (MIDC Boisar, Tarapur) invites applications from experienced professionals for the position of QA Manager to direct the site Quality Management System (QMS).
Key Roles & Responsibilities:
• Provide leadership and strategic direction to the site Quality Assurance department, ensuring end-to-end regulatory compliance.
• Oversee site QMS systems including Change Controls, Deviations, CAPA, Incident Management, and Market Complaints.
• Manage internal quality audits, vendor qualification programs, and lead customer and regulatory audit inspections (FDA/WHO-GMP).
• Review and approve validation protocols, master batch records (MBR/BPR), SOPs, and analytical method transfer dossiers.
• Foster a culture of quality, data integrity, continuous improvement, and operational excellence across the organization.
Candidate Profile & Requirements:
• Qualification: MSC, BSC.
• Experience: 1–3 Years in pharmaceutical quality management.
• Deep expertise in cGMP, ICH guidelines, regulatory compliance, and audit defense.
• Strong managerial, leadership, and technical writing skills.
• Gender Preference: Male & Female.
• Location: Boisar (MIDC Boisar, Tarapur).
• Compensation: 6L – 7L / year.
How to Apply:
Eligible and interested candidates are encouraged to apply directly through Jobrabit. Applications will be reviewed by Yukti Placement Services, and shortlisted candidates will be scheduled for interview screening in Boisar.
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