GMP Consultant – Life Sciences (Flanders)

About the role

ALTEN Belgium is seeking a GMP Consultant to join its Life Sciences consulting team in Flanders. The role involves working on challenging projects for pharmaceutical, medical device and biotechnology clients, helping them meet regulatory and quality standards.

Key responsibilities

• Provide consulting expertise on GMP‑related topics for life‑science clients.
• Support projects covering regulatory affairs, quality assurance, quality control, maintenance, automation, engineering, qualification & validation, data integrity, production, and project management.
• Collaborate with multidisciplinary teams to deliver optimal solutions and ensure compliance.

Required profile

• Experience in the pharmaceutical, medical devices or biotechnological industry.
• Background in one or more of the following areas: regulatory affairs, quality assurance, quality control, maintenance, automation, engineering, qualification & validation, data integrity, production, project management or project engineering.

Required skills

• Regulatory Affairs
• Quality Assurance
• Quality Control
• Maintenance
• Automation
• Engineering
• Qualification & Validation
• Data Integrity
• Production
• Project Management
• Project Engineering

What we offer

• Access to challenging projects with renowned clients.
• Continuous learning through ALTEN Academy and knowledge‑sharing events.
• Opportunities for career growth within an international network of experts.