Regulatory Project Manager, Regional Projects Team, CMC Excellence. Responsible for managing people aspects of a team, tracking team performance, and ensuring proper escalation for resource or quality considerations. Leads key activities to progress career and drives CMC strategy, coordinates, and prepares complex technical regulatory documents.
Requirements
- Master’s degree or higher in a relevant scientific discipline
- Experience in an international regulatory environment or working with multiple markets
- Sound understanding of pharmaceutical industry and regulatory processes with expertise in CMC area
- Project Management experience
- Capability to build and maintain a team
- Fluent English
- Strong interpersonal and communication skills
- Ability to perform multiple tasks, set the right priorities to deliver objectives on time
- Adapting to changing circumstances through priorities reassessment and a disciplined, logical work style
Benefits
- Performance with Choice
- Flexible working hours
- Established job in an international, well-known pharmaceutical company
- Opportunity to work in professional team playing crucial role in maintaining GSK portfolio on the markets
- Opportunity to work within GSK standards and documentation applied globally
- Wide range of benefits (Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus)
- Supportive & friendly working environment
