Production: Execute production batches, ensure GMP, manage documentation QA: Ensure cGMP, Issuance and retrievals and manage records. QC: Analyze biopharma samples & maintain Documentation R&D: Prepare stocks and buffers, extract proteins & analyze.
Design & oversee biosimilar clinical trials with CROs, ensuring regulatory compliance. Coordinate with medical advisors, manage IP logistics, submissions, and pharmacovigilance, and serve as main contact for government grant projects and reports.
Assist in installation, operation, and basic maintenance of utility and lab equipment. Support preventive maintenance schedules and update log sheets/documents. Coordinate with teams for work permits, safety practices, and vendor service. Follow GMP.
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