Job description
Opportunity Overview
We are offering international volunteer positions (VIE) for talented engineers and compliance specialists to support critical operations across our pharmaceutical sites in Belgium. These roles are ideal for early-career professionals seeking hands-on experience in a regulated industrial environment while gaining international exposure.
You will work within cross-functional teams on projects related to facility qualification, process optimization, regulatory compliance, safety, and capital investments.
Available Profiles & Key Responsibilities
1. CQV / Process Engineer (Commissioning, Qualification & Validation)
* Support the execution of CQV protocols (IQ/OQ/PQ) for equipment, utilities, and processes.
* Assist in process validation (PPQ, CPV) and technical transfer activities.
* Collaborate with engineering and quality teams to ensure compliance with GMP and regulatory standards.
* Contribute to documentation (protocols, reports, change controls).
2. Manufacturing Support / GMP Compliance Engineer
* Provide technical support to manufacturing units to ensure operational efficiency.
* Investigate deviations, support CAPA implementation, and participate in internal audits.
* Ensure adherence to GMP, safety, and quality standards across production lines.
* Assist in continuous improvement projects (Lean, Six Sigma).
3. EHS Engineer (Environment, Health & Safety)
* Implement and monitor EHS programs in line with local and international regulations.
* Conduct risk assessments, safety audits, and incident investigations.
* Promote a strong safety culture through training and awareness campaigns.
* Support sustainability initiatives and environmental compliance (waste, emissions, energy).
4. CAPEX Engineer – Utilities / Automation / Electrical
* Participate in the design, planning, and execution of CAPEX projects (new equipment, facility upgrades).
* Focus on utilities (WFI, HVAC, compressed air), automation (SCADA, PLC), and electrical systems.
* Coordinate with vendors, contractors, and internal stakeholders.
* Ensure projects meet budget, timeline, and compliance requirements (GAMP, GMP).
-----------------------------------
Who Are We Looking For?
* Nationality: Open to EU citizens (VIE program eligibility criteria apply – administered by Business France).
* Education: Bachelor’s or Master’s degree in Chemical, Mechanical, Electrical, Automation, Environmental Engineering, or related field.
* Skills & Qualities:
o Strong interest in the pharmaceutical, biotech, or life sciences industry.
o Basic understanding of GMP, validation, or industrial safety (training or internship experience accepted).
o Technical aptitude and problem-solving mindset.
o Fluency in English and French or Dutch.
o Adaptability, teamwork, and willingness to work in a regulated environment.
What We Offer
* A unique international experience under the VIE program.
* Monthly allowance, health insurance, travel coverage, and return ticket at the end of the mission.
* Mentorship and professional development within a global organization.
* Opportunity to work on high-impact projects in a cutting-edge pharmaceutical environment.
* Potential for future career opportunities within the group.
Why joining us?
Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees.
Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutions sectors on impactful missions.
International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe.