Manufacturing Engineer (ref. 2335)

Vacature

• Implement improvements and participate in projects • Manage and oversee the input and maintenance of recipes/formulas in EBS (Masterdata) to ensure accuracy and compliance with regulatory standards • Understand the process and user requirements driven by process maps / flows in preparation for developing or updating EBR designs. • Drive and support EBR design validation activities (lifecycle documentation generation, configuration/design testing and qualification) • Understanding how process and user requirements are converted into specific

Profiel

Bachelor’s degree or equivalent experience. 2-3 years’ relevant (process engineer / MES specialist) experience within a Pharmaceutical/GMP Manufacturing Site. Excellent knowledge of manufacturing processes. Good experience with supporting users. Experience with writing and execution CSV documentation / protocols for MES. GMP experience.