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Open nowPosted 33 hours ago

Commissioning & Qualification Equipment Engineer | Pharma | Beerse

SELECT PROJECTS (Select)

Where
Turnhout, Belgium
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Your applicationOpen nowCommissioning & Qualification Equipment Engineer | Pharma | BeerseSELECT PROJECTS (Select) · Turnhout, Belgium

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  4. 21.9%14 days
  5. 36.9%30 days
  6. 59.0%60 days
This job: posted 33 hours ago

The posting

As a Commissioning & Qualification Equipment Engineer, you are responsible for preparing, maintaining and executing qualification documentation for GMP-critical equipment, utilities and systems. You ensure that all documentation complies with applicable GMP requirements and internal quality standards. You work closely with C&Q Leads, Subject Matter Experts and project teams to support qualification projects from initiation through completion. Besides document preparation, you also participate in qualification testing and follow-up activities. Your work plays an important role in ensuring that systems remain in a validated and compliant state. Fortunately, we can count on you for:

  • Writing qualification documentation including URS, SRS, IA, DQ, IQ, OQ, PQ, QSR and Validation Master Plans
  • Executing and documenting qualification tests for equipment, utilities and systems
  • Assessing the impact of changes, deviations and discrepancies on qualification activities
  • Coordinating document reviews, approval flows and signature processes
  • Following up punch list items and qualification actions until closure
  • Supporting internal and external audits and inspections
  • Managing document archiving in accordance with GMP and GDP requirements

You are structured, quality-minded and eager to learn. You communicate effectively with different stakeholders and enjoy working in a team-oriented GMP environment. At the same time, you are capable of independently managing documentation and qualification activities.

What you bring

  • Bachelor's or Master's degree in a scientific or technical field such as Industrial Engineering, Biochemistry, Biotechnology or Pharmaceutical Sciences
  • Strong interest in the pharmaceutical industry and GMP-regulated environments
  • Excellent technical writing and documentation skills
  • Experience with engineering systems, utilities or manufacturing equipment is an asset
  • Fluent in Dutch and English, both written and spoken

Posting text belongs to the employer. Removal requests: contact us.

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