Our client is a leading organization in the life sciences sector dedicated to developing innovative therapeutic solutions. They focus on improving human health through scientific excellence, advanced technologies, and high-quality standards. The environment is dynamic, collaborative, and strongly quality-driven, offering employees opportunities to contribute to impactful projects.
Role descriptionAs an Associate Scientist, Compliance Management, you will play a key role within the Strategic Operations group, part of the Analytical Development department. You will ensure compliance with GMP standards by managing documentation, supporting quality processes, and collaborating with stakeholders across the department. This role is ideal for a detail-oriented professional who enjoys working in multidisciplinary environments and contributing to continuous improvement.
Key responsibilities- Review and lead document revisions
- Manage Change Controls
- Process non-conformance and CAPA records
- Maintain close communication with stakeholders
- Manage training curricula for Analytical Development employees
- Perform self-inspections within the department
- Design and implement quality and compliance improvements
- MLO-4
- Experience with cGMP
- Affinity and experience with (laboratory) systems such as COMET, TruVault, and SUMMIT
- 2–5 years of experience with compliance management activities
- Strong interpersonal skills and ability to build positive stakeholder relationships
- Experience in a quality-driven environmentStrong communication skills in English and Dutch (written and verbal)
Are you interested and do you want to apply for this role, please fill out your application via the apply button below and contact Margarida Louro.
#J-18808-Ljbffr€50000 - €70000 monthly