ASolution Pharmaceuticals Pvt. Ltd.

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.