Company Introduction
Cadila Pharmaceuticals operates formulation facilities supplying regulated domestic and international pharmaceutical markets.
Core Responsibilities
- Review batch manufacturing records using approved checklists before document closure.
- Verify in process control entries against master manufacturing documents.
- Inspect manufacturing and packaging areas using line clearance formats.
- Issue controlled quality documents through document issuance registers.
- Record observations from shop floor checks in quality monitoring logs.
- Archive completed records in compliance filing systems.
Skills and Technical Exposure
- Batch manufacturing records and control forms.
- Line clearance checklists and inspection formats.
- Controlled document management systems.
- In process quality monitoring registers.
- Good manufacturing practice documentation.
Experience Context
- Work setting is a formulation manufacturing plant with multiple dosage forms.
- Scale covers routine batch documentation and shop floor verification.
- Without this role, batch release documentation remains incomplete.
How to Apply
Share your updated CV to jimit.sharma@cadilapharma.com
