Commissioning & Qualification Equipment Engineer | Pharma | Beerse

As a Commissioning & Qualification Equipment Engineer , you are responsible for preparing, maintaining and executing qualification documentation for GMP-critical equipment, utilities and systems. You ensure that all documentation complies with applicable GMP requirements and internal quality standards. You work closely with C&Q Leads, Subject Matter Experts and project teams to support qualification projects from initiation through completion. Besides document preparation, you also participate in qualification testing and follow-up activities. Your work plays an important role in ensuring that systems remain in a validated and compliant state. Fortunately, we can count on you for: • Writing qualification documentation including URS, SRS, IA, DQ, IQ, OQ, PQ, QSR and Validation Master Plans • Executing and documenting qualification tests for equipment, utilities and systems • Assessing the impact of changes, deviations and discrepancies on qualification activities • Coordinating document reviews, approval flows and signature processes • Following up punch list items and qualification actions until closure • Supporting internal and external audits and inspections • Managing document archiving in accordance with GMP and GDP requirements You are structured, quality-minded and eager to learn. You communicate effectively with different stakeholders and enjoy working in a team-oriented GMP environment. At the same time, you are capable of independently managing documentation and qualification activities. What you bring • Bachelor's or Master's degree in a scientific or technical field such as Industrial Engineering, Biochemistry, Biotechnology or Pharmaceutical Sciences • Strong interest in the pharmaceutical industry and GMP-regulated environments • Excellent technical writing and documentation skills • Experience with engineering systems, utilities or manufacturing equipment is an asset • Fluent in Dutch and English , both written and spoken