Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of over 4.5 billion US Dollar. Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe.
Post : Executive - QC
Job Description :
1. To procure the laboratory standards according to the requirements.
2. Daily work allocation based on monthly and daily schedule.
3. Analysis of finished product and stability samples.
4. To receipt of all laboratory standard and maintaining the inventory, records and labeling according to the procedure.
5. Qualification of Working Standards and management of Laboratory standards (Like – Reference Standards/Primary Standards/Calibration Standards, etc.) in QC Lab.
6. Initiation of change control, Lab event, deviation etc. in track wise.
7. To performed periodically Calibration, Preventive maintenance, Performance verification and Qualification of instruments.
8. Issuance & receiving of HPLC/GC Column.
9. Raising of the work request in SAP for Breakdown of instrument/equipment/area, maintaining temp/RH etc.
10. Daily recording of Temperature & RH (Testo Saveris) of QC laboratory (including refrigerator, Dee freezer).
11. Responsible for integrity, accuracy and adequacy of the analysis performed.
12. To qualify the Working Standard vials for routine usage, issuance and Destruction of the same after the validity and maintain the records.
13. Periodic review and Verification of existing stock against the latest catalogue of respective pharmacopeia.
14. To ensure destruction of expired standards as per SOPs.
15. Initiate deviation, lab event, OOS in track wise and participate in investigation.
16. To participate and contribute in internal & external Audits.
17. Ensure archival of all type of records related to Quality control department.
18. Recording Analytical data in SAP & Preparation of Certificate of analysis.
19. To follow and ensure compliance to cGMP and EHS standards in the QC laboratory.
20. Any other assignment by lab incharge/Manager Quality control from time to time.
Additional Information
Qualification : M.Pharm, B.Pharm, M.Sc
Location : Mohali
Industry Type : Pharma / Healthcare/ Clinical research
Functional Area : Quality Control
End Date : 30th August, 2022
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