Posted:4 days ago|
Platform:
On-site
Full Time
1. 20+ years of experience in highly regulated plants, Tablet/capsule/pallets/OSD is must, injections preferred.
2. Should have excellent MHRA and EUGMP Profile with multiple successful audit exposures.
3. In QA Should be well versed with Updates in ICH Q9 guidelines and in QC Should be well versed with Updates in ICH Q2R2 Analytical method validation.
4. Should have large team size handling experience.
5. Should have proven stability.
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