Sr. Executive; QC
Opsonin Pharma Limited
Total des années d'expérience :20 years, 6 Mois
1. Maintaining of GLP and cleaning in Laboratory.
2. To carryout in-process, Intermediate & Finished product checking to
ensure that products are produced as per approved specifications.
3. Analyze raw materials, samples from different sources as per
requirements specification by using appropriate equipment & approved
test procedures.
4. Compile documents including export documents to ensure quality of the
documentation.
5. Preparation of working standards by following approved procedures.
6. Analytical Method Development and validation.
7. Performing stability study test & taking part in validation team.
8. Performing Calibration of Analytical Instruments.
9. Any other responsibilities assigned by the higher authority.
In Master's degree I stood 5th position in my University
