Company Introduction
Sun Pharmaceutical Industries Limited is a global pharmaceutical manufacturer focused on delivering high quality medicines through regulated manufacturing sites and compliant systems.
Core Responsibilities
- Review batch manufacturing records using approved master batch documents and controlled logbooks.
- Perform in process checks on sterile filling lines using sampling plans and inspection checklists.
- Verify cleaning records through equipment log sheets and line clearance forms.
- Observe media fill runs by checking intervention records and environmental monitoring sheets.
- Examine finished product samples through visual inspection booths and approved defect catalogs.
- Document batch release decisions through controlled release notes and archival files.
Skills and Technical Exposure
- Sterile manufacturing areas including clean rooms, laminar airflow units, and isolators.
- Environmental monitoring tools such as settle plates, contact plates, and particle counters.
- Media fill protocols, aseptic gowning qualification records, and validation reports.
- Controlled documentation systems, batch record formats, and quality review checklists.
- Visual inspection aids, defect classification charts, and sampling tools.
Experience Context
- Work is carried out inside injectable manufacturing plants with classified clean room environments.
- Daily exposure includes multiple sterile batches, routine sampling, and controlled equipment usage.
- Without this role, batch documentation gaps, inspection failures, and regulatory observations increase.
How to Apply
Share CV at disha.chauhan@sunpharma.com
