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
For more information, contact Jurjen Wilschut: 088 00 211 22 // jurjen@checkmark.nl
Vacancy Number: 8584
Our client in Amsterdam is the leading provider of specific analytical inspection systems used for the analysis of pharmaceutical products. The team in the Netherlands consists of 25 people serving the pharmaceutical industry.
Wat wij bieden- 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