Validation engineer

☞ Panda International

Vue: 80

Jour de mise à jour: 19-11-2025

Localisation: Geel Antwerp

Catégorie: Production/Opération

Industrie: Medical Equipment Manufacturing

Niveau: Associate

Type d’emploi: Full-time

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le contenu du travail

Cleaning Validation Engineer (MSAT Team)

About the Role

We are looking for an experienced Cleaning Validation Engineer to join our Manufacturing Science and Technology (MSAT) team.

In this role, you will focus on cleaning validation within a GMP-regulated pharmaceutical environment, ensuring that all cleaning processes meet the highest quality and compliance standards. You will lead validation activities, manage documentation, support audits, and help introduce new products and equipment into the validation program — driving operational excellence and regulatory compliance.

Key Responsibilities

  • Prepare, execute, and maintain cleaning validation documentation, including protocols, reports, and studies.
  • Evaluate and approve proposed changes; manage and prioritize cleaning validation projects.
  • Support internal and external audits and ensure timely closure of findings.
  • Lead validation activities for New Product Introductions (NPI) and new equipment.
  • Identify and report deviations, investigate root causes, and implement corrective and preventive actions (CAPAs).
  • Collaborate closely with Manufacturing, Quality, and Engineering teams to ensure robust and compliant processes.

Key Competencies

  • Proven expertise in API manufacturing and cleaning validation.
  • Strong understanding of validation principles and statistical methods.
  • In-depth knowledge of GMP and regulatory expectations for cleaning validation.
  • Excellent project management, planning, and organizational skills.
  • Ability to manage complexity, multiple priorities, and tight deadlines.
  • Strong communication and interpersonal skills across all organizational levels.
  • Experience with systems such as eLIMS, truVAULT, COMET, PRX, CRB, SAP, PASx, Minitab, CPV Automation is a plus.

Requirements

  • Master’s degree in (Bio)Sciences, Engineering, or Life Sciences.
  • Fluency in Dutch and English (written and spoken).
  • 2–4 years of relevant experience in pharmaceutical manufacturing or validation.

???? Interested?

Let’s connect!

Reach out to:

Sandro Alves

???? s.canelas@panda-int.com

???? +31 6 3150 1862

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Date limite: 19-12-2025

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