Project Engineer (Pharmaceuticals)

TL;DR

Project Engineer (Pharmaceuticals): Supporting the design, construction, and optimization of advanced manufacturing facilities with an accent on production systems, automation, and validation in GMP environments. Focus on leading CAPEX projects, executing IQ/OQ/PQ validation, and implementing MES/SCADA solutions.

Location: Belgium. Candidate must have EU citizenship.

Company

Independent technology consulting firm providing guidance and solutions to businesses across 60 countries.

What you will do

• Lead CAPEX investment projects for production facilities and utilities, managing scope, budget, and stakeholders.
• Execute IQ/OQ/PQ validation activities for equipment, utilities, and computerized systems.
• Design and implement MES, SCADA, and PLC automation solutions to support Industry 4.0 initiatives.
• Ensure continuous compliance with GMP and GxP regulatory standards.
• Coordinate the installation of manufacturing infrastructure and equipment.

Requirements

• EU citizenship (mandatory requirement for the VIE program).
• Bachelor's or Master's degree in Engineering (Chemical, Mechanical, Electrical, Automation, or Industrial).
• 3–5 years of experience in regulated industries (Pharma, Biotech, Life Sciences, or Medical Devices).
• Fluent English proficiency.

Nice to have

• Proficiency in French and/or Dutch.

Culture & Benefits

• International environment with a community of over 110 nationalities.
• Access to the internal Amaris Academy with 250+ training modules.
• Agile culture promoting intrapreneurship and fast career growth.
• Engagement in ESG and social impact projects through the WeCare Together program.
• Vibrant workplace with frequent internal events and team buildings.

Hiring process

• Brief virtual or phone introductory call to discuss motivations.
• Average of 3 interviews with line managers and team members.
• Potential technical assessment or case study depending on the specific role.