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Vie Pharmaceuticals

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Amaris Consulting

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Location:
Belgium , Brussels

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Category:
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Contract Type:
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Salary:

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Job Description:

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.

Job Responsibility:

  • 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)
  • 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)
  • 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)
  • 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)

Requirements:

  • Bachelor's or Master's degree in Chemical, Mechanical, Electrical, Automation, Environmental Engineering, or related field
  • Strong interest in the pharmaceutical, biotech, or life sciences industry
  • Basic understanding of GMP, validation, or industrial safety (training or internship experience accepted)
  • Technical aptitude and problem-solving mindset
  • Fluency in English and French or Dutch
  • Adaptability, teamwork, and willingness to work in a regulated environment
What we offer:
  • International experience under the VIE program
  • Monthly allowance
  • Health insurance
  • Travel coverage
  • 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

Additional Information:

Job Posted:
May 15, 2026

Work Type:
On-site work
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