Originally Gujarat based Company presence of 35 years in Pharma formulation having own marketing setup as well as 3rd party/loan licence activity at Gujarat and Dehradun plant.
Post: Assistant Manager- Q.A.
Job Description:
Preparation of documents as per Schedule-M and WHO guidelines which includes:
* Preparation of MFR and BMR/BPR of Product dealt with.
* Preparation of NEW SOP and reviewing of OLD SOP’s.
* Carryout validation of Products in terms of process and analysis.
* Calibration and validation of instruments as per WHO guidelines.
Candidate Profile:
Total 7 to 8 years of which 3 to 4 years at senior position in pharma industry.
- Exposure of preparation of documents pertaining to Q.C. instruments calibration and/or validation./schedule M/ WHO.
- Sound knowledge of syrups, suspension & solutions and tablets.
- Sound knowledge of dispersible / film coated tablets and dry syrup
- Sound Knowledge of Air / Water / HVAC advantageous.
Additional Information:
Experience: 7-8 years
Location: Dehradun
Education: B.Pharm, M.Pharm, B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QA
Last Date: 2nd Feb, 2012
Apply/Send resume at, dipak@hemadun.com, hr@hemadun.com
See All B.Pharm Alerts M.Pharm Alerts M.Sc Alerts Dehradun Alerts
See All Other Jobs in our Database
.png)
