Program Management Specialist

Key Responsibilities: Manage and execute CDMO projects from initiation to delivery, ensuring adherence to timelines, budgets, and quality standards. Act as the primary point of contact for internal stakeholders, ensuring smooth communication and alignment on project objectives. Collaborate closely with the Site Head, R&D, Manufacturing, Quality, Supply Chain, and Regulatory teams to ensure project milestones are achieved. Monitor project progress, identify risks, and implement mitigation plans to ensure on-time and in-full delivery. Prepare and present regular status reports and updates to senior management. Drive process improvements to enhance project efficiency and client satisfaction. Required Qualifications & Skills: Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Chemical Engineering, or related field. 4-6 years of experience in managing projects in CDMO/Pharmaceutical companies is a must. Strong understanding of CDMO operations , including R&D, tech

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