Position: Entry level

Job type: Full-time

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Job content

Job description:

We are looking for a motivated Validation Engineer who will be responsible for the documentation of mechanical systems and equipment, as well as performing design qualifications and, in a later phase, executing validation tests (IOQ) on these systems.

Main responsibilities:

  • Prepare and maintain validation documentation for mechanical systems and equipment
  • Perform design qualification activities
  • Execute and document validation tests (DQ – FAT – IOQ – PQ)
  • Ensure compliance with applicable regulations and standards
  • Collaborate with multidisciplinary teams to optimize validation processes

Profile of the ideal candidate

Required qualifications and skills:

  • Preferably 2 - 3 years of experience in validation
  • Knowledge of compliance and GDP (Good Documentation Practices)
  • Knowledge of GMP (Good Manufacturing Practice) guidelines
  • Strong documentation skills

Desired experience (nice-to-have):

  • Experience with design qualification processes
  • Background in mechanical validation
  • Experience within the pharmaceutical industry

Personality profile:

  • Critical mindset: Ability to critically evaluate processes and systems
  • Structured approach: Capable of seeing the big picture while paying attention to details
  • Accurate and methodical in working style
  • Strong communication skills for effective collaboration with the engineering department
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    Deadline: 13-01-2026

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