レベル: Mid-Senior level

ジョブタイプ: Full-time

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仕事内容

Join a leading organization in the pharmaceutical industry, where your expertise will contribute to the enhancement of cleaning validation processes. This is an opportunity to play a vital role in ensuring the quality and compliance of manufacturing operations.

We are seeking an experienced Cleaning Validation Engineer who will become a specialist in cleaning technologies and processes. If you are adept in validation and project management within a GMP production environment, we want to hear from you.

  • You develop and validate cleaning processes for equipment and tools.
  • You collaborate with other cleaning validation engineers to enhance cleaning technologies.
  • You understand technical aspects of cleaning processes, hardware, and software.
  • You lead improvements in cleaning processes for new product or equipment introductions.
  • You handle deviations and urgent issues to maintain operational continuity.
  • You participate in periodic process reviews and sampling programs to ensure compliance.
  • You can be a site topic lead, contributing to above-site discussions with cleaning validation experts.

Requirements

  • You hold a Higher Scientific Degree (Pharmaceutical Sciences, Bioengineer, Industrial Engineer).
  • You have at least 3 years of relevant experience in validation or project management within a GMP production environment.
  • You possess hands-on experience in regulated pharmaceutical manufacturing.
  • You are knowledgeable about cleaning and CIP processes.
  • You are analytical and project-minded.
  • You have excellent communication skills for engaging with team members at various levels.
  • You are a team player with a strong focus on customer needs.
  • You exhibit outstanding influencing and problem-solving skills.
  • You are fluent in both Dutch and English (verbal and written).
  • You are open to flexible working hours to support production continuity.
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締切: 13-01-2026

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