IMP Production Process Engineer — Lean & GMP Expert

Astek

Luik

Sur place

EUR 70 000 - 110 000

Plein temps

Il y a 13 jours
Générateur de candidature

Une candidature complète en une minute — un CV et une lettre de motivation personnalisés, prêts à être envoyés.

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Avantages offerts par ce poste

Company car
Petrol card
Meal vouchers
Group insurance
Hospitalization

Résumé du poste

Astek Belgium is seeking a Process Engineer to strengthen IMP production site design at Alleur and St Pieters Leeuw, joining our pharma-focused consulting team.

You will analyze physical, human, and information flows, identify risks and bottlenecks, and design end-to-end workflows aligned with GMP/ISO 9001 standards; you will also draft the roadmap for a new site with capacity for up to 20,000 patients.

Qualifications

  • Engineering degree in industrial, biotech, supply chain, or related field.
  • 5–8+ years as Senior Consultant in IMP/Pharma, lean optimization and flows.
  • Experience in GMP/regulated environments; ISO 9001 knowledge.

Responsabilités

  • Analyze IMP production site workflows and map end-to-end processes.
  • Identify risks, bottlenecks, and cross-contamination points; propose improvements.
  • Design blueprints for a new IMP site with capacity up to 20,000 patients.
  • Develop risk matrices, KPIs, and implementation roadmaps.
  • Define quality certifications and infrastructure needs for future site.

Connaissances

Production area design (IMP, Pharma)
Lean/industrial optimization
Continuous improvement
Logistics and pharmaceutical flows
Regulated GMP environments
ISO 9001 / GMP knowledge
French & Dutch communication
MS Office skills

Formation

Engineering degree (industrial, biotechnology, supply chain, or related)

Outils

MS Office

Description du poste

Astek Belgium is seeking a Process Engineer to strengthen IMP production site design at Alleur and St Pieters Leeuw, joining our pharma-focused consulting team.

You will analyze physical, human, and information flows, identify risks and bottlenecks, and design end-to-end workflows aligned with GMP/ISO 9001 standards; you will also draft the roadmap for a new site with capacity for up to 20,000 patients.

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