Senior Executive, Lab QA at Amneal India

Ahmedabad, gujarat, India -

Full Time

Start Date

Immediate

Expiry Date

13 Oct, 26

Salary

0.0

Posted On

15 Jul, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Data Review, Quality Assurance, LIMS, cGMP, GLP, ALCOA Principles, Method Validation, Stability Testing, Audit Trail Review, OOS Investigation, Computer System Validation, Vendor Qualification

Industry

Pharmaceutical Manufacturing

Description

1. Review analytical data for Raw Materials (RM), Packaging Materials (PM), in-process samples, Finished Products (FP), stability samples, working standards, reference standards, and other test samples. 2. Review and approve Certificates of Analysis (COAs) for RM, PM, in-process samples, FP, stability working standards, reference standards, and other test samples. samples. 3. Review SOPs, STPs, specifications, and other laboratory documents. 4. Verify the accuracy of data entered in LIMS and manual documentation systems. 5. Review protocols and reports related to analytical method transfer, validation, verification, and waiver activities. Review analytical raw data associated with method transfer, validation, and verification studies. 6. Review and approve daily verification, calibration, and qualification records of laboratory instruments and equipment. 7. Review and approve Computer System Validation (CSV) documents. 8. Review instrument logbooks, calibration records, and third-party calibration reports. 9. Review and approve the audit trail reports for Empower and non-CDS systems. 10. Review stability schedules, stability protocols and stability reports. 11. Ensure data integrity and compliance with ALCOA principles and documentation practices. Verify analytical records for compliance with GLP and cGMP requirements. 12. Review investigations related raw data and report i.e. OOS, OOAL/OOT, deviations, incidents, and change controls. 13. Review vendor qualification reports and related documentation. 14. Review reduced testing reports and related documentation. 15. Review analytical data and COAs received from contract testing laboratories. 16. Review and approve preparation records of reagents, mobile phases, diluents, impurity solutions, and other laboratory solutions. 17. Review analytical raw data for analyst qualification and approved. 18. Verify compliance of laboratory activities through documentation review. Additional Responsibilities:

Responsibilities

Responsible for reviewing and approving analytical data, Certificates of Analysis, and laboratory documentation to ensure compliance with quality standards. Oversees instrument calibration, stability reports, and investigations into deviations or out-of-specification results.