| Location | Leiden, South Holland, Netherlands, Netherlands |
|---|---|
| Business Sector | Pharmaceutical |
| Contact email | |
| Job ref | 26579 |
| Published | about 17 hours ago |
Job Role: Associate Scientist – Compliance Management
About the Role:
We are seeking a motivated Associate Scientist to join the Compliance Management team within the Strategic Operations group of Analytical Development. In this role, you will ensure high standards of quality and compliance across lab and production operations, supporting documentation, training, inspections, and continuous improvement initiatives. You will work closely with cross-functional stakeholders to maintain GMP compliance and support advanced therapeutic development.
Key Responsibilities:
Review and lead revisions of documents to ensure compliance.
Manage Change Controls and oversee non-conformance/CAPA records.
Maintain and coordinate training curricula for AD employees.
Perform self-inspections within the department.
Design and implement improvements regarding quality and compliance.
Collaborate closely with internal and external stakeholders.
Support oversight of lab and production systems, equipment, and automation solutions.
Key Competencies:
Strong attention to detail and accuracy.
Proactive, solution-oriented, and team-player mindset.
Excellent communication and interpersonal skills (English and Dutch).
Ability to build strong relationships with stakeholders.
Experience working in a quality-driven, GMP environment.
Requirements:
MLO-4 or equivalent higher vocational education.
2–5 years of experience in compliance management or quality-related activities.
Experience with cGMP standards.
Familiarity with laboratory and data management systems (COMET, TruVault, SUMMIT).
Developed interpersonal and stakeholder management skills.
Practical Information:
Location: Leiden, The Netherlands
Start Date: ASAP
Work Model: On-site
Interested or know someone who might be?
Send your CV or inquiries to e.cabral@panda-int.com.