Global Program Management - Manufacturing

At Biocon Biologics, we are creating a model for the future of healthcare for all. We are a leading company in the biosimilars revolution where patients come first. Our ambition is to impact a billion lives and we do this by fostering a culture of affordable innovation, patient centricity and disruptive thinking. We are a multicultural global company where employees have a purpose and passion to work closely with partners and patients. We have proven end to end expertise in the field of biosimilars, from its development, manufacturing, clinical development, regulatory approvals to commercialization. We have a long-term commitment to bring high quality affordable biosimilars to patients all over the globe.Job ResponsibilitiesOperations Management of Manufacturing activitiesResponsible for tracking and reporting manufacturing KPIs – Monthly, Quarterly & Annual reportingWeekly MIS preparation & monthly report updateHigh level understanding of Supply Network Management.Responsible for oversight on key issuesResponsible for tracking expenses monthly & QuarterlyFollow the Governance Structure and Escalation Matrix as defined within Global Program Management functionScope and Schedule management: Follow the annual plan & budgetTrack the Plan Vs Actual and report the variance.Pro-actively track and report delays & issuesMonitor the progress through-out the schedule (MSP, Office timeline)Stakeholder management: Effectively co-ordinate with cross functional teams within the organization and also with the partner teams for program deliverables. Manage communications, escalation & problem solving to ensure project deliverables stay on trackBudget: Plan the cost centre budget (Annual/Quarterly/Monthly).Budget forecasting for the Fiscal yearFinalize, Track and Report the Plan vs ActualsNegotiation with the service providers for the program related activities.Monitor/control project progression to ensure project is completed on schedule and within budget. Anticipate and provide visibility to internal/external stakeholders for scope/cost creep & revisionRegulatory:Participate in contributing to regulatory strategy.Liaise with RA team and finalize the regulatory pathway for variation filingsLegal:Liaise with the Legal team and ensure readiness of CDA, MSA, SOW etc. prior to the project execution.Logistics: Liaise with Procurement and Logistics teams to facilitate and track the shipments (project related materials, test items/drugs, testing/biological samples)Procurement: Liaise with procurement team for the availability of project related consumables, equipment & other critical reagents required for the programNote: This role is not for the candidate with experience in IT.