Work from Office
Full Time
1. Good knowledge about QC compliance GLP related activity.
2. Review all specification & testing procedures and test data sheet for raw materials, intermediates, finish goods, stability, in process and packing materials.3. Good knowledge about verification of COAs as per specification.4. Review of analytical data and audit trail prior to batch release of finished products and stability data.5. Maintain records of daily monitoring temperature & humidity of stability chamber.6. Good knowledge about batch release related activity.7. Good knowledge of ensure QC specification and analytical method are confirming to the tested pharmacopoeia & customer requirements.8. Good knowledge about stability data to support retest or expiry dates and storage condition on APIs & intermediates where appropriate. 9. Control/reserve sample management.10. Involvement regulatory/customer audits.
Preferred candidate API industry
Ipca
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