Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies.
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.
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.
Education:
Master’s degree in Pharmacy or Chemistry.
Minimum 2 to 5 years in project management within CDMO or Chemical or pharmaceutical industry.
Strong understanding of regulatory requirements and cross-functional coordination.
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.
Education:
Master’s degree in Pharmacy or Chemistry.
📩 Interested candidates may send their CV to:
hr.hiring@bpin.eurofinsasia.com
🔁 Feel free to share or refer suitable candidates in your network.
Originally posted by Eurofins. View original posting
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