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Merck seeks a Quality Data Associate Specialist for its Haarlem facility to manage and ensure quality data and processes in pharmaceutical manufacturing. The role involves supporting product release, regulatory compliance, and new product introductions across multiple quality systems and disciplines.

Responsibilities

Support implementation of guideline changes through Veeva and Change Control processes
Lead or participate in new product introductions with focus on quality aspects
Review and approve masterdata in systems such as ZERT, ZERP, and ZDSB
Conduct material control reviews and deviation investigations as needed
Write and maintain QMS procedures and quality standards documentation

Requirements

Bachelor's or Master's degree in pharmacy, life sciences, process technology, or chemistry
Minimum 1 year relevant quality experience in GMP environment
SAP, LIMS, and Veeva experience preferred
Knowledge of packaging technology and pharmaceutical registration preferred
Fluent in Dutch and English, both written and spoken
Analytical, detail-oriented, and self-directed work approach

Quality Data Associate Specialist

Begin met je e-mail