GSK is a global biopharma company that aims to positively impact the health of 2.5 billion people by the end of the decade. We are seeking a Project Manager, CMC Regulatory Affairs to join our team. As a Project Manager, you will be responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK products.
Requirements
- Chemistry, Manufacturing and Controls (CMC) regulatory affairs or product development experience
- Degree in life sciences or related scientific discipline
- Sound knowledge of drug development, manufacturing processes and supply chain
- Good time management skills
- Demonstrated knowledge of all relevant components of project management
Benefits
- Attractive reward package (annual bonus & awards for outstanding performance, recognition awards for additional achievements and engagement, holiday benefit)
- Hybrid working model (where GSK site are in Poland)
- Extensive support of work life balance (flexible working solutions, min. 2-3 days/week working form the office, health & well-being activities)
- Life insurance and pension plan
- Private medical package with additional preventive healthcare services for employees and their eligible family members
- Sports cards (Multisport)
- Possibilities of development within the role and company’s structure
- Personalized learning approach (internal trainings, mentoring, access to online training’ platforms: Keep Growing Campus, LinkedIn Learning, Business Skills, Harvard Manage Mentor, Skillsoft and external training)
- Supportive community and integration events
- Modern office with creative rooms, fresh fruits every day
