The Eurofins BioPharma Services Network of Companies is a first-class biopharmaceutical outsourcing services partner (Contract Research Organization - CRO), working with pharmaceutical, chemical, biotechnology, medical device, and cosmetic clients.
The network covers the whole chain of drug development thanks to an international network of laboratories and testing units with global reach, uniform QA systems, and high-quality services.
We are looking for a GMP Project Coordinator for our customer service team who will contribute to the significant growth of our business by:
Key Responsibilities
- End-to-end project leadership for Pharma Analytics: Analytical Development & Method validation, Dissolution, Chromatography, Particle Testing, Stability Storage, and related subcontracted services within the Eurofins Group
- Project planning and timeline management: define project plans, track milestones, manage POs, risks and forecasts, and report status to stakeholders
- Technical coordination: review and evaluate technical customer requests and create appropriate work packages and proposals
- GMP compliance: ensure correct execution of commissioned analytical work per GMP; contribute to audit readiness and continuous improvement
- LIMS configuration: map and configure projects in LIMS and support data integrity best practices
- Stakeholder management: coordinate interfaces between internal labs, clients, and external partners; support new project acquisition
- Quality system contributions: assist in authoring and maintaining SOPs and GMP documentation; support client, GMP, and regulatory audits
- Process optimization: identify and implement improvements to increase efficiency, quality, and throughput at the site