Act as a Project Lead for the assigned clinical trials while supervising CRAs in their functions of monitoring and administration of clinical trials. To manage service providers, CRO and Vendors, collect quotes budget proposals, summarize and present the same to the management team.
Working in aseptic process area for supervision and operation of filling and manufacturing activity. Handling of Complex of Microsphere formulation. Handling of Dry powder filling machine.
Knowledge of Production Planning, Co-ordination with Corporate Planning Team for smooth function, Scheduling of Manufacturing, Follow-ups with Inter-Departments for production activity.
responsible for overseeing day-to-day operations, ensuring compliance with regulatory standards, and driving continuous improvement across all processes. Oversee daily QC and microbiology operations, ensuring CGMP and regulatory compliance.
Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.
Infusion bags processing activities, In-process checks and Line Clearance activities, Handling of shift activities and manpower. Preparation of QRM, Incident and Investigation, OOL and OOS investigation, CC and CAPA, Protocols and CAPA closure reports.
Experience in Yeast Biology not limited to culture methods, strain modification, transformation and expression studies. Experience in Molecular Biology and Biochemical techniques, preferably in Saccharomyces Biology.
Demonstrated success in project management & experience with mentoring and coaching junior team members. Ability to act independently with a solutions-oriented and balanced approach to the grey areas.