Job Description
- Fair knowledge of unit operations in API manufacturing.
- Hands on experience in sampling of process validation and equipment cleaning validation.
- Hands on experience in reviewing executed documents - batch manufacturing records, batch packing records, dispatch activity.
- Working knowledge of equipment / utilities / area qualification activity.
- Knowledge of basic Quality System SOPs of Pharma QA, manufacturing
- Working knowledge of GMP requirements as per Schedule M, ICH Q7, Q9, Q10, 21 CFR Part 210 & 211, WHO and EU guidelines.
- Communication skills - Good spoken and written English.
- Computer literate (MSWord, MS Excel)
- Ready to work in shifts.