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5.0 - 10.0 years
5 - 11 Lacs
Dholka
Work from Office
Role & responsibilities 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. Preferred candidate profile Must have experience in Biopharma
Posted 3 months ago
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