Requalification/Revalidation Engineer
Il y a 1 jour
Geel, Flanders, Belgique
EFOR
Temps plein
Gratuit avec email ou Google
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
Gratuit avec email ou Google
En continuant, vous acceptez nos Conditions d’utilisation & Politique de confidentialité.
Are you an experienced validation professional ready for your next challenge? We are seeking a Requalification/Revalidation Engineer to join the team at our Geel site in Belgium.
About the Role
As a Requalification/Revalidation Engineer, you’ll play a key role in the ongoing remediation program, supporting the requalification of critical equipment—including autoclaves, washers, and controlled temperature units (CTUs, such as refrigerators and freezers). You’ll also be involved in the qualification and validation of biologics process equipment, offering flexibility to support both requalification and potential revalidation activities as project needs evolve. What we’re looking for:
• Solid experience with equipment requalification and/or revalidation, especially for autoclaves, washers, CTUs (refrigerators/freezers)
• Direct experience with qualification and validation in biologics manufacturing is a strong plus
• Good understanding of GMP and regulatory requirements
• Strong documentation and technical writing skills
• Ability to adapt to changing project scopes and priorities Join a dynamic remediation programme at one of the world’s leading pharmaceutical companies, and contribute to quality improvement in a state-of-the-art biologics manufacturing environment.
About the Role
As a Requalification/Revalidation Engineer, you’ll play a key role in the ongoing remediation program, supporting the requalification of critical equipment—including autoclaves, washers, and controlled temperature units (CTUs, such as refrigerators and freezers). You’ll also be involved in the qualification and validation of biologics process equipment, offering flexibility to support both requalification and potential revalidation activities as project needs evolve. What we’re looking for:
• Solid experience with equipment requalification and/or revalidation, especially for autoclaves, washers, CTUs (refrigerators/freezers)
• Direct experience with qualification and validation in biologics manufacturing is a strong plus
• Good understanding of GMP and regulatory requirements
• Strong documentation and technical writing skills
• Ability to adapt to changing project scopes and priorities Join a dynamic remediation programme at one of the world’s leading pharmaceutical companies, and contribute to quality improvement in a state-of-the-art biologics manufacturing environment.