Quality Data Associate Specialist in Haarlem, Nederland

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