QA Supervisor

Preparation, review and approval of SOPs and GXP documents.

Issuance, review, approval and retrieval of BMR/BPR.

Follow GMP guidelines in the production area.

Exposure of audit inspection of USFDA and/or other regulatory agencies.

To handle training management system.

To handle the Process validation & cleaning validation activity.

To handle risk assessment, change control system, deviation, CAPA, OOS & OOT.

Line clearance, IPQA, Sampling activity.

We are inviting candidates with a valid US Visa to apply for job opportunities for our manufacturing facility in the United States.

Applicants who do not hold a U.S. visa but are keen to work at a U.S. manufacturing unit may also apply.