Project Management Specialist

As an experienced professional in the CDMO industry with a background in M.Sc. with any chemistry/B. Pharma/M. Pharm, you will be responsible for the following key tasks: - Develop comprehensive project plans, including detailed timelines, milestones, and resource allocation. Drive project teams through all phases of the project lifecycle. - Ensure strict adherence to global and local regulatory, quality, and safety guidelines such as FDA, EMA, and Good Manufacturing Practices (GMP). - Proactively identify, assess, and mitigate potential project risks, and develop contingency plans to address unforeseen issues, delays, or safety concerns. - Prepare detailed project budgets and financial forecasts, monitor expenditures, and optimize resource utilization to ensure financial constraints are met. - Ensure all customer deliverables and expectations are met in full and on time, as outlined in the Project Charter. - Track, maintain, and report On-time In Full (OTIF) performance for all CDMO projects. - Lead and coordinate cross-functional teams, including R&D, Quality, Analytical, Production, and Regulatory personnel, to ensure clear communication and alignment across departments. - Serve as the primary point of contact for internal and external stakeholders, including customers, senior management, investors, and third-party vendors. Provide regular, detailed reports on project status, risks, and performance metrics. - Conduct regular reviews to ensure all project deliverables meet required standards and client expectations. - Maintain thorough project documentation, including protocols, reports, and lessons learned, for governance, compliance, and future reference. The work location for this role is at Honour R&D (CDMO), Bonthapally, Hyderabad. As an experienced professional in the CDMO industry with a background in M.Sc. with any chemistry/B. Pharma/M. Pharm, you will be responsible for the following key tasks: - Develop comprehensive project plans, including detailed timelines, milestones, and resource allocation. Drive project teams through all phases of the project lifecycle. - Ensure strict adherence to global and local regulatory, quality, and safety guidelines such as FDA, EMA, and Good Manufacturing Practices (GMP). - Proactively identify, assess, and mitigate potential project risks, and develop contingency plans to address unforeseen issues, delays, or safety concerns. - Prepare detailed project budgets and financial forecasts, monitor expenditures, and optimize resource utilization to ensure financial constraints are met. - Ensure all customer deliverables and expectations are met in full and on time, as outlined in the Project Charter. - Track, maintain, and report On-time In Full (OTIF) performance for all CDMO projects. - Lead and coordinate cross-functional teams, including R&D, Quality, Analytical, Production, and Regulatory personnel, to ensure clear communication and alignment across departments. - Serve as the primary point of contact for internal and external stakeholders, including customers, senior management, investors, and third-party vendors. Provide regular, detailed reports on project status, risks, and performance metrics. - Conduct regular reviews to ensure all project deliverables meet required standards and client expectations. - Maintain thorough project documentation, including protocols, reports, and lessons learned, for governance, compliance, and future reference. The work location for this role is at Honour R&D (CDMO), Bonthapally, Hyderabad.