Manager - Quality Assurance (OSD & Injectable) - IPQA, Packing & Manufacturing (Formulations) Job Purpose To ensure compliance with cGMP, regulatory requirements, and quality standards by overseeing In-Process Quality Assurance (IPQA) activities during manufacturing and packing of Oral Solid Dosage (OSD) and Injectable formulations. The role is responsible for maintaining product quality, ensuring process compliance, and supporting successful regulatory inspections and audits. Major Responsibilities Lead and manage IPQA activities for OSD and Injectable manufacturing and packing operations. Ensure compliance with cGMP, SOPs, data integrity, and regulatory guidelines (USFDA, MHRA, EU GMP, WHO, etc.). Perform line clearance, in-process checks, and stage-wise quality verification during manufacturing and packaging. Review Batch Manufacturing Records (BMR), Batch Packing Records (BPR), logbooks, and other GMP documentation. Investigate deviations, OOS/OOT, market complaints, and quality in...