QA Compliance Specialist (GMP)

Location: Geleen, Netherlands; fully site-based. Relocation assistance is available for eligible candidates and their families.

Annual base pay: EUR 41,250–57,750.

Company

hirify.global operates more than 30 sites across five continents and manufactures medicines and life-science products for customers worldwide.

What you will do

• Support the site Quality Management System, including documentation, training administration, quality records, and related systems.
• Review and manage deviations, CAPAs, change controls, risk assessments, and other quality processes.
• Coordinate supplier and service-provider qualification, supplier complaints, vendor change notifications, and supplier lifecycle activities.
• Support internal, customer, and external audits and regulatory inspections to maintain inspection readiness.
• Deliver or support GMP and compliance training and contribute to quality culture initiatives.
• Identify and implement improvements to quality systems and compliance processes.

Requirements

• Bachelor’s degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related discipline, or equivalent relevant experience.
• Working knowledge of GMP principles, Quality Management Systems, and quality compliance requirements.
• Strong organization, documentation, communication, collaboration, and problem-solving skills.
• Ability to manage multiple priorities and deadlines and work with stakeholders across functions.
• Proficiency with Microsoft Office.
• Experience in a GMP-regulated pharmaceutical, biotechnology, medical-device, or similar quality environment is advantageous.

Nice to have

• Experience with SAP, document management systems, or learning management systems.
• Experience with supplier management, compliance, and continuous improvement activities.

Culture & Benefits

• Agile career development and a dynamic working culture.
• Inclusive and ethical workplace with a focus on collaboration, accountability, excellence, passion, and integrity.
• Compensation programs that recognize high performance.
• Opportunities to develop expertise across quality systems, compliance, supplier management, and GMP activities.
• Collaborative environment focused on continuous improvement and meaningful impact.