Executive QA

Abbott Laboratories

Aussicht: 106

Update Tag: 24-05-2024

Ort: Baddi Himachal Pradesh

Kategorie: Produktion / Betrieb

Industrie:

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Jobinhalt

1. Control sample management and compliance of all document and procedures related to control sample area in STARLIMS.
2. To maintain documentation of Control Sample Area.
3. To receive Control sample, maintain record of receiving.
4. Visual Inspection and destruction of control sample as per schedule. Records maintenance of the inspection and destruction.

5. Monitoring temperature through eurotherm software and recoding the temperature humidiity through manual data logger.

6. Preparation & Review of SOPs in DARIUS.

7. To prepare Master Documents i.e., Site Master File, Quality System Manual

8. Filling of Implementation Review Form (IRF), Follow-up of the task generated in gap assessment, verification of updated document.

9. Closure of the Implementation Review form (IRF) in DARIUS system.

10. Filling of the document and up-dation of logbooks with Uncontrol print and mail communication to Regional QA for closure.

11. Up-dation of Internal Audit observation/ Response report in report in Track wise system Audi-Q.

12. Follow-up of the task generated from Internal Audit. Verification of evidence and closure in the Track wise system Audi-Q.

13. To update Annexures in Site Master File, Quality System Manual.

14. To maintain proof book for External Audit observations.

15. To ensure effective execution and closure of respective tasks of GEMBA walk rounds at Baddi.

16. To co-ordinate and support in investigation activity of exceptions.

17. To ensure the self-training in ISO train within the stipulated time frame.

18. To ensure compliance of current Good Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity compliance.
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Frist: 08-07-2024

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