Job Description
Roles and Responsibilities
1. Analysis of FG/ RM/PM/IP/stability/Water/hold time study & other analysis related in Quality control dept.
2. Maintain, Monitor &Implementation of cGLP & cGMP as per latest norms.
3. All quality control related documents, records, raw data shall be reviewed.
4. Sampling of incoming Raw materials, packing materials & miscellaneous materials.
5. Calibration of Equipments / Instruments.
6. Destruction of respective records & QC Samples like Raw materials reference samples, & RM /PM/IP/FG/stability/Water/hold time study left over samples.
7. Reporting of OOS, OOT, deviations, change control Laboratory Incidence during analysis activity.
8. To comply Internal and External Audit Observations.
9. Preparation and maintenance of Analytical data sheets and Excel spread sheets.
Desired Candidate Profile
Experience - 8 to 10 Yrs in reputed Pharma company
Qualification MSc./ B.Pharm/ M.Pharm
Job Location - Jejuri, Pune.
Note Candidate will work in Nigeria plant for 01 year on rotational basis
Perks and Benefits
Best in the industry