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02/09 Neeta Saji
Associate Consultant at Cornerstone International FGroup

Views:105 Applications:3 Rec. Actions:Recruiter Actions:0

Analyst - Stability Studies/Formulations - Pharma (8-15 yrs)

Overseas/International/Ireland Job Code: 32635

Stability Studies Analyst - Formulations - Pharma

We are looking for Stability Analyst ( QC Stability Analyst) from Quality Control dept.

Responsibilities :

1. To carry out analytical testing on finished products & raw materials using the correct procedures in order to comply with GMP, Health and Safety, SOP's and environmental and regulatory requirements while ensuring we meet our customer's needs.

2. To provide technical support as required by management.

3. Displays the capability to learn and understand methods showing competency in the following technical areas: HPLC, GC, IR, UV, dissolution & physical testing.

4. Maintain and follow all relevant Standard Operating Procedures (SOP's).

5. Full analysis of finished product and stability sample (tablets, Granules, Liquid, veterinary drenches etc) in a timely manner using appropriate analytical techniques with limited analyst related OOS.

6. Calibration and maintenance of laboratory equipment as per calibration procedures.

7. To maintain all laboratory logbooks, notebooks & associated documentation to GLP.

8. Review and approve QC documents as required.

9. To bring to the notice of the team leader/supervisor any discrepancies, deviations or non conformances in testing or work practice.

10. Display ability and follow up on Corrective Actions.

11. Sending out samples for external analysis when requested.

12. Participating in internal/External Audits.

13. Liaising with external suppliers/vendors in relation to QC consumables.

14. Ensure existing quality procedures are followed and where appropriate suggestions/change control forms are prepared so that the quality system will be continuously improved.

15. To adhere to any agreed internal laboratory rota tasks.

16. To maintain good housekeeping and hygiene within the laboratory.

17. Adherence to laboratory safety measures at all times highlighting areas for improvement

18. Ensuring that laboratory is kept tidy and that GLP/GMP standards are adhered to at all times

19. Ensure records pertaining to QC are all kept up to date and filed properly.

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