Launch Excellence: Validation Project Manager

Pauwels Consulting

Puurs-Sint-Amands

Sur place

EUR 60 000 - 80 000

Plein temps

Il y a 2 jours
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Résumé du poste

Pauwels Consulting in Belgium seeks an experienced Validation Specialist to lead GMP validation for new product introductions. The role covers documenting processes, risk assessments, and cross-functional collaboration to ensure regulatory compliance and successful implementation.

You will coordinate validation activities, manage investigations, and drive process improvements with a strong emphasis on quality and timelines. Fluent Dutch and good English are required.

Qualifications

  • Master's degree in a relevant scientific field.
  • 3+ years in a GMP environment with validation and risk assessment focus.
  • Strong planning and project coordination for complex validation projects.
  • Analytical, technical writing and problem-solving with a quality mindset.
  • Proactive team player who can work independently or with others.
  • Fluent in Dutch with good knowledge of English.

Responsabilités

  • Validate and document processes for formulation, filling, shipping, and packaging.
  • Execute and document urgent quality investigations.
  • Perform comprehensive risk assessments and define mitigation measures.
  • Support and implement process and system changes for product introductions.
  • Provide overall project management, including coordination, planning, and progress reporting.
  • Collaborate with cross-functional teams to ensure service standards and goals.

Connaissances

GMP validation
Risk assessment
Project coordination
Technical writing
Analytical skills
Dutch language
English language
Team player

Formation

Master's degree in Bio-engineering / Pharmacy / Biochemistry / Biotechnology or related field

Description du poste

Pauwels Consulting in Belgium seeks an experienced Validation Specialist to lead GMP validation for new product introductions. The role covers documenting processes, risk assessments, and cross-functional collaboration to ensure regulatory compliance and successful implementation.

You will coordinate validation activities, manage investigations, and drive process improvements with a strong emphasis on quality and timelines. Fluent Dutch and good English are required.

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