GMP Validation Engineer — Life Sciences Consulting

Avertim

Antwerpen

On-site

EUR 45,000 - 70,000

Full time

25 hours ago
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Benefits offered by this job

Dynamic environment
Young team
European network
Career development
Competitive pay

Job summary

Avertim is seeking a Validation Engineer to ensure equipment, systems, and processes comply with GMP and regulatory requirements. You will collaborate with Quality, Engineering and Operations teams to maintain validated states and drive continuous improvement in a consulting environment.

You will join a dynamic European network and support clients across Life Sciences, leveraging your validation expertise and hands-on approach to deliver robust documentation and successful audits.

Qualifications

  • Master’s degree in a scientific or technical field (engineering, life sciences, chemistry, etc.).
  • 1 to 5 years of experience in validation and/or a GMP-regulated environment.
  • Solid understanding of GMP principles.
  • Structured, detail-oriented and hands-on.
  • Fluent in English and Dutch (French is a plus).
  • Willing to work in a consulting environment.

Responsibilities

  • Perform qualification and validation activities for equipment, utilities, processes and cleaning.
  • Prepare and review validation documentation such as URS, risk assessments and IQ/OQ/PQ protocols and reports.
  • Support CSV activities where applicable.
  • Manage deviations, CAPAs and change controls.
  • Support internal and external audits and inspections.
  • Ensure compliance with GMP guidelines and quality standards.

Skills

Validation
GMP knowledge
Documentation
Cross-functional
Quality systems

Education

Master's degree

Job description

Avertim is seeking a Validation Engineer to ensure equipment, systems, and processes comply with GMP and regulatory requirements. You will collaborate with Quality, Engineering and Operations teams to maintain validated states and drive continuous improvement in a consulting environment.

You will join a dynamic European network and support clients across Life Sciences, leveraging your validation expertise and hands-on approach to deliver robust documentation and successful audits.

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