5+

Packaging Material Vendor evaluation & Vendor development. Assessment of High Speed lines for future volumes and Expansion. Packaging Validation activities for enhancing operational efficiency.

Plan, execute, control and carry out projects with outsource CDO/CMO/CDMO partners to support the process of approval and launching new products in Canada market.

Mammalian and Microbial (Upstream Process): Media preparation, Filtration, Aseptic technique, Inoculum Handling, Handling of SU bioreactor/RM, Perfusion technology, upstream analytical instruments. Handling of SS Fermenter, Continuous centrifuge

Ointment, General Manufacturing & Sterile Manufacturing, Granulation, Compression, Coating, Capsule

Experience in handling equipment like Reactor, Centrifuge, ANFD, Multimill, Micronisation, Sparkler filters, Technology Transfer for scale up at Pilot Plant. Handled finished goods store, Dispatch, Export, Domestic Knowledge of E-Way Bill, customs, GST.

Regulated markets and currently working as a shift incharge. Experience in compression, granulation and should possess expertise in Quality Management System (QMS) production.

M.Pharma, M.Sc. in Life Sciences, MBA ; Organizing promotional programs & participation in exhibitions for greater brand visibility including fixing meetings around conferences. Meet, exceed the business closure targets from assigned territory.

Sterile manufacturing Suspension/emulsion /PFS / BFS as well as SKID operation. Should have experience in Aseptic process, complex manufacturing, Exposure to CIP/ SIP SKID, QMS.

Compile registration dossiers for submission to various health authorities like – USA, Canada, Europe, Australia and Israel. Prepare responses to deficiency letters received from various agencies.