Company Introduction
Lupin Limited is a global pharmaceutical manufacturer focused on formulation development, regulated manufacturing, and large-scale supply of complex dosage forms.
Core Responsibilities
- Prepare Validation Master Plans and Cleaning Validation Master Plans using approved templates and document control systems.
- Review validation protocols and reports for equipment, utilities, and facilities using controlled QA checklists.
- Perform equipment qualification activities for manufacturing and packing lines using IQ, OQ, and PQ documentation.
- Conduct temperature and relative humidity mapping using data loggers and approved study formats.
- Carry out utility qualification for compressed air, nitrogen gas, and purified water systems using sampling tools.
- Maintain HVAC qualification records, periodic review logs, and validation summary files.
Skills & Technical Exposure
- Validation Master Plans, cleaning validation protocols, and qualification reports.
- Data loggers, temperature probes, and relative humidity monitoring instruments.
- IQ, OQ, PQ formats for equipment and utility qualification.
- Compressed air, nitrogen gas, purified water, and HVAC system documentation.
- Audit readiness files, validation trackers, and controlled document archives.
Experience Context
- Work is performed at a pharmaceutical manufacturing site supporting regulated dosage form production.
- Daily involvement covers multiple production lines, utilities, and storage areas.
- Without this role, validation files lapse, audit readiness weakens, and equipment release timelines stall.
How to Apply
suhailkhan1@lupin.com