Quality Manager GMP

As a Quality Manager GMP, you will be responsible for developing, implementing, and improving the quality system (GMP, ICH, ISO) of our client. You will play a key role in maintaining high-quality standards and lead processes such as audits, non-conformities, and change management. In this role, you will also be responsible for leading and coaching the QA team, consisting of two QA Officers. Your key responsibilities include:

• Implement, maintain, and improve the quality system in accordance with GMP, ICH, and ISO standards
• Lead, guide, and support the QA team (2 QA Officers) in daily operations and continuous improvement
• Organize and execute internal audits and supplier audits
• Monitor and report on the effectiveness of the quality system to management
• Manage documentation and archiving systems
• Analyze and resolve non-conformities and implement CAPAs
• Maintain quality agreements with customers and suppliers

• Long term position, which starts with a one year contract directly at the company
• Salary indication from € 5000,- to € 6400,- gross per month based on a full-time position
• 8% holiday pay
• Position for 32 – 40 hours/week
• Dayshift

For the position of Quality Manager GMP we are looking for a quality-driven professional who takes ownership, inspires others, and knows how to translate GMP principles into daily practice. Furthermore, we ask for:

• Hbo, MSc or PhD in Life Sciences, Chemistry, or a related field
• At least 3 years of relevant experience in a QA and/or leadership role within a pharmaceutical GMP environment
• Proven leadership skills or the ability and ambition to lead a QA team
• In-depth knowledge of EU GMP and quality management systems
• Strong analytical, organizational, and problem-solving abilities
• Excellent communication skills in Dutch and English
• Residence in the Amsterdam area and possession of a BSN (citizen service number)