Role & responsibilities
- Handle IPQA activities for OSD manufacturing and packing operations.
- Perform in-process checks and line clearance as per approved SOPs/BMR/BPR.
- Review BMR/BPR, logbooks, checklists and other GMP documents.
- Monitor manufacturing processes and ensure compliance with cGMP, SOPs and regulatory requirements.
- Handle deviations, OOS/OOT, CAPA and change control related to production activities.
- Ensure compliance with data integrity and documentation practices.
- Coordinate with Production, QC, QA and Engineering departments for timely resolution of quality issues.
- Support internal, customer and regulatory audits, including USFDA inspections.
- Ensure proper implementation of GMP and QMS requirements on the shop floor.
- Review and approve cleaning, environmental and process-related records as applicable.

Preferred candidate profile

Candidates from OSD formulation plants with exposure to USFDA-approved facilities / regulatory audits preferred.

📌 Assistant Manager IPQA (Baddi)
🏢 Acme Formulation
📍 Baddi