Production QMS
7 days ago
Role & responsibilities
- Handling of QMS for drug substance of bacterial products. Should have good process understanding of upstream and downstream unit operations.
- Experience to handle QMS documents such as deviation, Change control, Investigations through Track-wise software.
- Should have experience on audit compliance, Regulatory guidelines and knowledge on documentation such as SOP, BMR preparation.
- 5-8 years of experience on QMS and compliance, Documentation role along with good understanding about manufacturing process operations of bacterial and recombinant vaccine and biological therapeutics.
Preferred candidate profile
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