Role Summary
Responsible for managing client-sponsored projects from initiation to closure in a CDMO environment. Ensure timely execution, resource coordination, regulatory compliance, and effective communication with sponsors and internal teams.
Key Responsibilities
- Initiation – Update project details in systems, share cost documents, and conduct internal kick-off.
- Planning – Prepare project charter, risk register, Gantt chart, and communication plan.
- Execution – Ensure RM procurement, monitor timelines, and coordinate regulatory requirements.
- Control – Track scope, schedule, and cost; manage risks and change requests.
- Closure – Capture lessons learned, submit closure report, obtain sponsor acknowledgment, and release team.
Eligibility & Education
Education:
- Master’s degree in Pharmacy or Chemistry.
Experience:
- Minimum 2 to 5 years in project management within CDMO or Chemical or pharmaceutical industry.
- Strong understanding of regulatory requirements and cross-functional coordination.
Skills:
- Proficiency in project management tools (MS Project, Gantt charts) and excel work books.
- Excellent communication and stakeholder management.
- Ability to manage budgets, timelines, and risks effectively.