Associate Principal Scientist leading CMC initiatives in a global biopharmaceutical company. Driving strategic planning and delivery of key transformation projects across cross-regional functions.
Responsibilities
Lead, support or project manage the design and implementation of cross-regional or functional business strategies
Support communication on initiatives progress and implementation, keeping the organization informed and supporting associated change management activities
Coordinate and contribute to the delivery of the Regional CMC strategic plan, operating model transformation initiatives, and key priorities
Support the management of Regional CMC priorities, roadmap, scorecards, and dashboards
Digital transformation, including supporting Digital capabilities build in the Regional CMC team
Strengthen Regional CMC’s partnerships with other GRACS and broader enterprise stakeholders across regions
Requirements
Minimum of 5 years’ experience in regulatory affairs
2+ years’ experience in project and change management
Strong collaboration and communication skills
Ability to manage complex projects and initiatives with limited supervision
Strong digital skills and familiarity with digital tools and platforms
Enterprise mindset with an ability to think strategically across the organization
Experience in managing cross-functional teams and working with strategic partners
Experience with CMC regional regulatory strategies is preferred though not essential
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