Validation Engineer

About the role:

For an international pharmaceutical organization in the Boxmeer region, we are looking for a  Validation Engineer  with a strong technical or scientific background. In this role, you will support validation activities for equipment, cleaning and sterilisation processes within a regulated pharmaceutical environment. You will work on project‑based validation activities and contribute to the quality, compliance and reliability of production processes. This is a hands‑on role for someone who combines technical understanding with strong documentation skills and who enjoys working in a cross‑functional setting.

Key responsibilities:

As Validation Engineer, you will be responsible for supporting and executing validation activities within ongoing projects. Your responsibilities include:

Working on cleaning validation and sterilisation validation studies

Authoring validation master plans, protocols and final reports

Updating SOPs and validation‑related documentation

Executing validation studies according to approved protocols

Analysing validation data and translating results into clear documentation

Identifying and resolving technical issues during study execution

Working closely with Engineering, Quality, Manufacturing and other technical teams

Ensuring validation activities are performed in line with GMP requirements and internal procedures

Your profile:

We are looking for someone with:

A Bachelor’s or Master’s degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences or a related discipline

Experience with equipment validation, cleaning validation and/or sterilisation validation

Knowledge of GMP and validation documentation requirements

Strong technical writing skills

The ability to analyse validation data and document findings accurately

Strong communication skills in English, both written and spoken

A structured, accurate and proactive way of working

The ability to work independently as well as in cross‑functional project teams

Experience with in a pharmaceutical, biotech or other regulated production environment is preferred

Visa sponsorship is not possible

Candidates should live within commuting distance of Boxmeer

What you can expect:

This role offers the opportunity to contribute to important validation projects within a highly regulated pharmaceutical environment. You will work with experienced colleagues across multiple disciplines and receive direction and support while taking ownership of your own validation activities. You will be part of a professional and quality‑driven environment where technical accuracy, documentation and collaboration are key. Interested? Are you a technically strong Validation Engineer with experience in equipment, cleaning or sterilisation validation?

We would be happy to tell you more about this opportunity.

Apply directly or contact Talentmark for more information.

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