Equipment Qualification Engineer | Life Sciences

Location: On-site in Diegem, with work at the client's Geel site in Belgium

Company

hirify.global is a global engineering and technology transformation partner delivering R&D, engineering, digital, cloud, data, and AI services across more than 50 countries.

What you will do

• Support equipment qualification and requalification in a GMP-regulated pharmaceutical manufacturing environment.
• Prepare, execute, and review IQ, OQ, and PQ documentation according to GMP/GxP requirements.
• Contribute to commissioning, qualification, and validation activities for utilities, facilities, and process equipment.
• Identify deviations, follow up on CAPA activities, and support remediation plans for qualification gaps.
• Support inspection-readiness activities and maintain audit-ready documentation and processes.
• Collaborate with Engineering, Quality, Manufacturing, and Validation teams while working autonomously on-site.

Requirements

• At least 3 years of experience in equipment qualification, validation, or a related role in pharmaceutical or biopharmaceutical manufacturing.
• Hands-on experience with IQ/OQ/PQ protocols, CQV methodologies, and GMP/GxP documentation.
• Experience with utilities, facilities, and process equipment in a regulated manufacturing setting.
• Strong understanding of deviation management, CAPA processes, and remediation planning.
• Fluency in English and Dutch is required for communication with local site teams in Geel.

Culture & Benefits

• Participation in Impact Together Week, supporting sustainable and inclusive initiatives.
• Mentoring programs supporting professional growth and the empowerment of women in engineering.
• Free access to learning platforms and content from Harvard Business Review, Coursera, Pluralsight, Udemy, Microsoft, AWS, Google, and other providers.