Qc Officer

1 day ago

Ankleshwar, India CP HR Services Pvt.Ltd Full time

**Position**:QC Officer**

**Qualification-**:BSC/MSC in chemistry

**Experience**:

- Minimum 2 years in API pharma

**Location**:

- Ankleshwar, Gujarat

**Gender**:

- Only male

**Job Description-**

1. Perform all QC activity as per defined SOP and document it on time.

2. To perform analysis as per specification and testing method and as per pharmacopeia monograph.

3. Responsible for analysis of raw material, In-process, equipment cleaning verification, vendor qualification and finished product sample with accuracy on time.

4. Responsible for Daily calibration and as per schedule calibration of QC instrument.

5. Responsible for preparation and maintain enough Standard solution, Reagent and volumetric solution.

6. Responsible for preparation of certificate of analysis after analysis.

7. To perform raw and packing material sampling, analysis and paste approved label after review of documents.

8. To assist the Head QC in investigation of OOS results.

9. To maintain the stability chamber for temperature, humidity, and recording.

10. To ensure that the Laboratory is cleaned as per frequency as given in SOP.

11. Responsible for stability sample charging and analysis as per schedule.

12. Responsible for sampling and analysis of water.

13. Responsible for sending samples to an outside approved lab for analysis in which facility is not at site.

14. Maintain glass ware, Chemical and Reagent stock for regular use.

15. Responsible for inform about any OOS, Deviation, incident Related to analysis to Head QC.

16. Responsible for inform any out of calibration (OOC) to Head and help in investigation.

17. Responsible for arranging to collect lab waste in specified container and send for destruction to ETP.

18. Responsible for arranging of all chemical, segregate and store as per SOP.

19. Responsible for following Safety rules in lab.

20. To attain on job training and periodic training program.

21. Follow the Company HR rules and discipline in terms of regularity and timing.

22. Follow the company quality policy.

23. Believe in teamwork for the growth of the company.

24. Always make helping nature to colleagues and superior.

25. At the time of internal audit, customer audit or regulatory audit provide support for documents and required information.

26. Must follow defined basic GMP/GLP and compliance requirement within the company premises.

27. To ensure usage of proper PPE’s (Personnel Protective Equipment) wherever required.

28. To control waste generation and spillage of reagents, chemicals etc. during analysis.

29. Any other work allocated by department head.

**Job Types**: Full-time, Permanent

Schedule:

- Day shift

**Experience**:

- Quality control: 2 years (preferred)

Work Location: In person

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