Description

You will manage automation projects in regulated pharmaceutical environments, ensuring compliance with GMP, Eudralex, and FDA standards.

You will define functional and technical requirements for automation systems and implement solutions that align with quality standards. Travel to client sites in Brussels, Wavre, Braine-l'Alleud, Puurs, Beerse, Genval, Ghent, Leuven, or other key locations is required.

Responsibilities

• Define functional and technical requirements for automation systems.
• Ensure all implementations comply with GMP, Eudralex, FDA, and EHS standards.
• Identify and implement technical solutions that align with GMP quality standards.
• Travel to client locations in Belgium for project execution.

Required Skills

• Master's degree in engineering or equivalent qualification.
• 1 to 5 years of experience as an Engineering Project Manager.
• Proficiency in English and French at a professional level.
• Knowledge of Archestra, Emerson DeltaV, Rockwell, or Siemens systems.
• Experience with MES programs.
• Working knowledge of SQL databases.
• Compliance expertise in GMP, Eudralex, and FDA standards.

Preferred Skills

• Significant experience working within the pharmaceutical industry.

Key Skills

Education

Master's degree