
Program Management Specialist
2 weeks ago
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.
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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 transfer, and manufacturing processes.
- Excellent stakeholder management, communication, and problem-solving skills.
- Ability to work in a fast-paced, matrixed environment with multiple internal teams.
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