MES Quality Engineer | Life Sciences

Your role

We are looking for a skilled and detail-oriented QA Engineer to join the Supply Chain Quality team supporting a leading pharmaceutical manufacturing site in Geel. In this role, you will be responsible for the review and approval of Master Batch Records and Recipes, playing a vital part in ensuring the timely and compliant production of commercial APIs. You will work closely with both business and quality partners, contributing to a culture of continuous improvement and regulatory excellence.

In this role you will play a key role in:

• Reviewing and approving Master Batch Records for commercial APIs, ensuring accuracy, completeness, and full compliance with applicable cGMP regulations and internal quality standards
• Reviewing and approving Recipes within the PAS-X Manufacturing Execution System (MES), ensuring that all production steps are correctly captured and aligned with regulatory and procedural requirements
• Writing, reviewing, and approving relevant QA procedures, contributing to the maintenance and continuous improvement of the site's quality management system
• Providing hands-on support for optimisation projects and tasks within the QA Commercial Operations team, applying a solutions-oriented mindset to drive efficiency and quality improvements
• Building and maintaining strong collaborative relationships with business and quality partners, communicating clearly and effectively across teams to ensure alignment on quality and compliance matters

Your profile

• You hold a Bachelor's degree or higher in a scientific discipline such as chemistry, biology, pharmacy, engineering, or a related field
• You bring a minimum of 3 years of experience in the chemical and/or pharmaceutical industry, with a background in Supply Chain and/or Quality Assurance and a solid understanding of cGMP regulations
• You are proficient in the PAS-X Manufacturing Execution System (MES) and have a strong understanding of production systems and their operation; familiarity with Delta-V and/or knowledge of API manufacturing or cleaning validation is considered a strong advantage
• You are a proactive, independent professional with strong analytical and critical thinking skills, a quality-focused mindset, and the ability to manage multiple tasks while maintaining clear communication with key stakeholders
• You are fluent in English; proficiency in Dutch is considered an asset and will be advantageous in day-to-day collaboration at the Geel site

What you'll love about working here

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