Posted:3 days ago|
Platform:
Work from Office
Full Time
Working on unit operations related to upstream processing during DS Manufacturing.
GMP Documentation related to DS manufacturing.
Preparation of documents like SOPs, MMDs and QMS related documents like change control, deviation, CAPA, Risk assessment.
Preparation and maintenance of virus stocks.
Coordination with cross-functional team.
Involvement during regulatory audit preparation.
Must have experience in Biopharma
Cadila Pharmaceuticals
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