Executive QA - #978396


Date: 1 week ago
City: Ahmedabad, Gujarat
Contract type: Full time
Job Description

Followings will be the responsibilities of the position holder:

1. Compliance of current Good Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity compliance.

2. Manufacturing and Packing process compliance in accordance with approved BMR/BPR.

3. To carry out line clearance, In-process checks at the different stages of batch manufacturing and packing.

4. Collection of control samples / stability samples / validation samples / other samples (as applicable) and maintain their record.

5. Issuance of Batch records and review of executed batch documents.

6. Compliance of IPQA related SOPs and records.

7. Calibration of IPQA instruments and to maintain related records.

8. SOP training in ISO train of self-train within stipulated time.

9. To check and review the BMR/BPR, other related documents of finished goods.
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