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)