Responsibilities and duties
- Sampling and analysis of Raw materials, Packing materials, In process, Intermediate and Finished products
- Calibration of Quality Control instruments
- Conducting Stability/Holding time studies
- Handling of Reference Standards and qualification of Working Standards
- Analyst qualifications
- Analytical Method Validation.
- Management of Control samples (Retain sample)
- Conducting OOS investigations (Phase-1)
Required Experience, Skills and Qualifications
- 2-3 years experience in Pharmaceutical Quality Control
- M.Pharmacy/B.Pharmacy/M.Sc. (Chemistry)/B.Sc. (Chemistry)
- Experience in handling HPLC, GC and other Quality Control instruments preferred
- Good documentation skills with exposure to GLP, GDP and cGMP practices
- Experience in:
- Sampling and analysis
- Calibration
- Stability/Holding time studies
- Analytical Method Validation
- OOS investigations
Benefits
Competitive wages and benefits
Yearly bonus
Increments every year based on performance
Training
Lunch service
Commuting support
