Qualification / Validation Consultant

☞ Pauwels Consulting

Ver: 102

Día de actualización: 07-11-2025

Ubicación: Liège City Liège

Categoría: Seguro de Calidad / Control de Calidad

Industria: Staffing Recruiting

Posición: Mid-Senior level

Tipo de empleo: Full-time

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Contenido de trabajo

Job Title: Consultant – Validation & Qualification (Medical Devices)

Location: Liège, Belgium (Hybrid – 1 day remote per week)

Contract Type: Long-term mission

Job Description:

We are looking for a highly motivated Validation & Qualification Consultant to join our client, a leading company in the Medical Device industry located in Liège. The consultant will be responsible for performing equipment qualifications and process validations across the organization, ensuring compliance with applicable regulations and internal quality standards.

Key Responsibilities:

  • Plan, execute, and document qualification activities for all equipment within the company (IQ/OQ/PQ).
  • Perform process validation activities to ensure consistent performance and compliance.
  • Develop, review, and update validation protocols, test plans, and reports.
  • Ensure alignment with regulatory requirements (ISO 13485, FDA, EU MDR, GxP, etc.).
  • Collaborate with cross-functional teams (Quality, Production, Engineering, R&D) to support validation activities.
  • Identify and implement improvements to validation and qualification processes.
  • Participate in audits and inspections as a subject matter expert for validation.

Requirements:

  • Degree in Engineering, Life Sciences, Pharmacy, or a related field.
  • Proven experience in validation and qualification within the Medical Device or pharmaceutical industry.
  • Strong knowledge of regulatory standards (ISO 13485, EU MDR, FDA, GxP).
  • Hands-on experience with equipment qualification (IQ/OQ/PQ) and process validation.
  • Analytical mindset with strong problem-solving skills.
  • Excellent communication and documentation skills in English (French is a plus).
  • Ability to work independently and collaboratively in a multidisciplinary environment.

Offer:

  • Long-term assignment in a dynamic and innovative Medical Device company.
  • Hybrid working model: 1 day per week remote.
  • Opportunity to contribute to high-impact projects in a regulated environment.

What are we looking for?

Requirements:

  • Degree in Engineering, Life Sciences, Pharmacy, or a related field.
  • Proven experience in validation and qualification within the Medical Device or pharmaceutical industry.
  • Strong knowledge of regulatory standards (ISO 13485, EU MDR, FDA, GxP).
  • Hands-on experience with equipment qualification (IQ/OQ/PQ) and process validation.
  • Analytical mindset with strong problem-solving skills.
  • Excellent communication and documentation skills in English (French is a plus).
  • Ability to work independently and collaboratively in a multidisciplinary environment.

What do we offer?

Offer:

  • Long-term assignment in a dynamic and innovative Medical Device company.
  • Hybrid working model: 1 day per week remote.
  • Opportunity to contribute to high-impact projects in a regulated environment.
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Plazo: 22-12-2025

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