25/05/2020
• Well acquainted with all activities pertaining to Parenteral formulation (Liquid and Lyophilized Formulations) development techniques from literature survey, patent evaluation for product under development.
• Knowledge about the handling of Cytotoxic materials.
• Knowledge about the regulatory guidelines, safety aspects, GLP and GMP.
• Knowledge about the qualification of instruments
• Write SOPs, Protocols and Reports
• Maintain laboratory SOPs in a state of compliance.
• Ensure equipment is adequately qualified and maintained in accordance with cGMP requirements.
• Perform, track and monitor stability testing as required.
• Produce deliverables for assigned projects in a timely manner.
