MBR Editor

Are you ready for the next step in your career? As a technical specialist in the Life Science sector, you work on technologies that improve lives. You play a key role in the development and optimization of systems for drug production, medical devices and biotechnology, for example.

Your work is crucial to the success of these projects.

Responsibilities

• As a MBR Editor you are responsible for creating electronic batch records (EBRs) to support the introduction of new projects. 
• You create, edit, and proof electronic batch records to ensure high quality, accuracy, and compliance with defined editorial and GMP standards.
• You configure production processes within the MES system (PAS-X).
• You translate manufacturing processes into Master Batch Records (MBRs) within the MES environment.
• You collaborate closely with cross-functional teams to assess project requirements and ensure correct implementation in batch documentation.
• You ensure consistency and standardization across batch records and related documentation.
• You support projects throughout their full lifecycle, from initial setup through implementation and deployment in production.

Requirements

• Bachelor’s degree or equivalent through relevant professional experience.
• Experience in a GMP manufacturing environment. 
• Knowledge and hands-on experience with Master Batch Record (MBR) design in PAS-X or an equivalent MES system.
• Ability to work independently as well as collaboratively within a team, supported by strong interpersonal skills.
• Ability to work in a structured and plan-driven manner, with good time management and attention to detail.
• Strong written and verbal communication skills in both English and Dutch.

At STAR, your career is our focus. We connect you with challenging projects, offer personal guidance and create opportunities with clients you are excited about.

Together we make sure you get the most out of your career.