Team Member - IPQA

Role Overview: As a Team Member in IPQA for Injectables/OSD, you will be a skilled professional with over 5 years of experience in real-time monitoring of manufacturing and packaging processes. Your responsibilities will include line clearance, in-process checks, and reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure compliance with GMP and regulatory standards. You will also be involved in deviation handling, documentation, and providing audit support for injectable and oral solid dosage forms. Key Responsibilities: - Real-time monitoring of manufacturing and packaging processes - Conducting line clearance and in-process checks - Reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure compliance with GMP and regulatory standards - Handling deviations and maintaining documentation - Providing audit support across injectable and oral solid dosage forms Qualifications Required: - B.Pharm or M.Sc. in Chemistry or Microbiology - Minimum 5 years of experience in IPQA, BMR/BPR review, and pharmaceutical manufacturing Additional Details: Omit this section as there are no additional details provided in the job description.,