Posted:-1 days ago|
Platform:
Work from Office
Full Time
1. To Conducted in-process quality checks during Manufacturing Process.
2. To Monitored critical process parameters and ensured compliance with SOPs and BMR/BPR documentation.
3. To Performed line clearance, area cleanliness verification, and material reconciliation.
4. To Preparation of APQR (Annual Product Quality Review).
5. To Review of Batch Manufacturing Record & Batch Packaging Record.
B.Pharma/M. Pharma Candidate with relevant 2 to 7 years of experience of regulated Formulation Manufacturing Plant.
Ashish Life Science
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