Production Engineer Vaccines Filling
Contract onbepaalde duur
Flanders, [Belgium]
08 Aug 2025
Role Overview:
In the Vaccines department, raw materials are transformed into filled medicines.
The product goes through various production steps such as weighing, preparation, formulation, filling, freeze-drying, capping, inspection, storage, and transport. At every stage, the production team strives for the highest level of operational excellence.
As a Production Engineer for Filling - Freeze Drying - Inspection,
you monitor the efficiency, quality, and consistency of the production process within the department. You are responsible for the technical aspects of the operations and work closely with production and maintenance teams to resolve production issues and validate and implement new products and processes on existing production lines.
Scope of Work:
Responsible for the validation of new products and improvements on existing filling lines: validation documentation, production follow-up, operator training
Communicative and maintains a clear overview of all tasks. Coordinates implementations and ensures that the set deadlines are met
Identifies and analyzes bottlenecks, quality issues, and efficiency losses. Collaborates closely with production operators and all relevant departments
Shows interest in how equipment functions both technically and process-wise
Proactively safeguards the process quality thanks to a critical mindset
Independently investigates (quality) issues and proposes appropriate solutions
Responsible for writing and maintaining procedures and organizing and delivering training to operators
Requirements:
Must-have:
Background: Industrial Engineer, Civil Engineer, or Bioengineer
Strong planning and analytical skills with a keen interest in production technologies and processes
Strong analytical capabilities
Excellent interpersonal and communication skills
Works in an organized and accurate manner
Hands-on mentality
Stress-resistant
Flexible
Technical interest
Nice to have:
Experience in a similar position
Experience in a GMP environment