Analytical Strategy Project Planner

6 days ago

Dublin, Ireland Cpl Healthcare Full time

Overview
Are you a detail-oriented and adaptable project planner/manager with experience in the pharmaceutical industry?
We are looking for a Project Manager – Analytical Strategy Planner to join our client's Analytical Strategy & Lifecycle (ASL) team as a contractor on an initial 12 month contract.
In this role, you will drive analytical project planning, oversee execution of critical deliverables, and support commercialization projects across a diverse biologics portfolio.
This is a fantastic opportunity to apply your expertise in project management, analytical sciences, and CMC within a dynamic, cross-functional environment.
Responsibilities
Develop and manage integrated project plans, timelines, and capacity models across multiple brands.
Track milestones, ensure analytical CMC deliverables are met, and maintain alignment with global project timelines.
Monitor risks by maintaining the operational risk register and preparing contingency plans.
Lead book-of-work planning in collaboration with Analytical Product Leads and SMEs.
Coordinate financial and FTE resource forecasting for current and future analytical activities.
Communicate project progress through executive-level status reports and dashboards.
Drive process improvements and harmonized ways of working across brands.
Manage day-to-day operational activities including quality metrics, repository platforms, and team reporting.
Requirements
Bachelor's degree in a scientific discipline; advanced degree desirable.
4+ years' experience in the pharmaceutical industry, with at least 3 years in project planning/management in a GMP manufacturing environment.
Strong knowledge of project management methodologies, including risk, resource, and issue management.
Familiarity with analytical methods for biologics (e.g., iCIEF, HPLC, CE, Bioassay, ELISA, LC-MS).
Excellent organizational, analytical, and communication skills with proven ability to manage multiple priorities.
Biologics regulatory experience is a plus.
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