Minimum of 15 Years of Experience in Cell Culture Upstream Process
To lead Upstream team in Drug Substance Manufacturing Department.
To provide guidance and train the sub ordinates.
To Ensure cGMP principles are followed by team members. Responsible to Prepare / review protocols, reports, Batch Manufacturing Records, Standard Operating Procedures and Qualification Documents.
To comply with National and International quality and regulatory standards and always be ready for all kinds of internal and external audits.
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