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15.0 - 20.0 years
0 - 0 Lacs
ahmedabad
Work from Office
Job Title: Project Manager Global Contract Manufacturing (India CMO) Location: Manufacturing Site, Ahmedabad Experience Required: 15-20 years Educational Qualification: B. Pharm / M. Pharm with MBA or PMP certification Job Summary: This role is part of the Global Contract Manufacturing (GCM) team, responsible for managing projects across CMO/CDMO platforms for OSD, Injectables, and Complex Injectables targeting regulated markets such as the US, EU, Japan, Korea, and India. The ideal candidate will possess strong analytical and project management skills, with hands-on experience in SAP, launch coordination, and cross-functional collaboration with R&D, Supply Chain, Manufacturing, and Client teams. The role requires travel and on-site coordination. Key Responsibilities: Act as the primary point of contact for clients and internal stakeholders. Lead project management calls and ensure timely updates on milestones and deliverables. Develop and manage Work Breakdown Structures (WBS) , project charters, and stage-gate processes. Coordinate with cross-functional teams (Manufacturing, QA, QC, CQA, Supply Chain) for successful project execution. Support regulatory audits, tech transfers, and legal documentation (CDA, manufacturing agreements). Maintain project MIS, track forecasts, and manage commercial product launches. Conduct market research and develop business cases for potential out-licensing deals. Key Stakeholders: Client Teams: ADL, Manufacturing, QA, Supply Chain, Technical Leads Internal Teams (Zydus): Demand & Supply Planning, Production, QC, R&D, Regulatory Affairs Performance Indicators: Timely development of WBS, project charters, and technical evaluations. Achieve 85% OTIF for India CMO launches and 90% OTIF for commercial products. Accurate costing, PO management, and scenario planning for business deals. Regular client updates on project status and milestone achievements. Required Competencies: 810 years of experience, with 59 years in project management for regulated markets. Experience with injectable and OSD dosage forms. Familiarity with legal agreements (MSA, CDA, supply & quality contracts). Strong market research and competitive intelligence capabilities. Proven ability to manage cross-functional teams and complex project timelines. Excellent communication, presentation, and documentation skills. Proficiency in MS Office (Word, Excel, PowerPoint) and SAP. Preferred Attributes: Proactive, solution-oriented, and ready to take on challenges. Strong interpersonal skills and ability to work in a dynamic environment.
Posted 1 day ago
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