We are currently partnered with a leading global biopharmaceutical organisation to support the search for an experienced Analytical Project Manager to join their team on a high-impact Phase 1 vaccine project.
This is a part-time, 12-month contract opportunity with hybrid flexibility. The successful candidate will play a key role in managing analytical activities across external labs, coordinating project communications, and ensuring high-quality data handling in a regulated GMP environment.
Key Responsibilities
- Oversee analytical method development and review of stability data from external laboratories
- Manage communications between research, manufacturing, and quality stakeholders
- Lead deviation management and ensure CAPA processes are followed
- Support cross-functional project teams to ensure timely delivery of documentation and data
- Coordinate with clinical development teams to meet regulatory standards
Essential Skills and Experience
- Minimum 4 years’ experience in analytical project management
- Strong background in vaccines, ideally non-viral, antigen-based platforms
- Proven experience with analytical method development and GMP-compliant environments
- Experience handling data from external labs and managing stability programs
- Excellent communication skills and fluency in English
- Bachelor's or Master's degree in a relevant scientific discipline
This is an excellent opportunity for a detail-oriented validation professional looking to work at the forefront of biopharma manufacturing and contribute to high-priority commercial and technical activities.
To apply or learn more, please submit your CV or reach out directly for a confidential discussion.
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- Posted
- Jun 18, 2025
- Type
- Contract
- Level
- Mid-Senior
- Location
- Basel
- Company
- Hamlyn Williams
Industries
Categories
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3 roles aligned with this opportunity
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