MES Design Specialist
Solliciteren
Plaats
Brussel1000
Brussel
België
Contract
Vooltijds, Onbepaalde duurDatum gepubliceerd
2026-02-18Online to:
2026-04-19EUR 15.00 HOUR
MES Design Specialist
MES Design Specialist
Brussels area, Belgium
Introduction
At Nalys, we empower engineers to grow through exciting projects within leading life sciences environments. We are currently looking for a MES Design Engineer to support one of our pharmaceutical partners near Brussels.
In this role, you will contribute to the design, improvement, and maintenance of electronic Master Batch Records within a GMP‑regulated manufacturing context. If you are passionate about digitalizing production processes and ensuring high‑quality execution on the shop floor, this opportunity is for you.
Your Responsibilities
As an MES Design Engineer, you will be involved in activities such as:
Supporting the design and configuration of MES batch templates and production workflows
Translating process requirements into clear, compliant designs
Ensuring consistency, accuracy, and alignment with GMP and operational needs
Participating in the transposition and transformation of existing production documents into digital formats
Supporting updates, modifications, and improvements to existing MES recipes
Preparing and reviewing technical documentation, including rationales, change controls, and related quality documents
Working with engineering, production, QA, and validation teams to ensure smooth deployment of MES functionalities
Providing technical support during troubleshooting, testing, and qualification activities.
What You Bring
You hold a Bachelor's or Master's degree in Engineering, Life Sciences, IT, or a related field — or you've built equivalent technical expertise through hands‑on experience
You have at least one year of experience in the pharmaceutical or chemical industry, ideally in a role connected to digital manufacturing or production processes
You already have exposure to MES design, eMBR creation, or the digitalization of manufacturing workflows
You understand the fundamentals of GMP, validation practices, and process documentation
You are detail‑oriented, analytical, and comfortable collaborating with cross‑functional teams
You communicate fluently in English, and you can also work in French
You're confident using standard IT tools (Excel, Word, documentation platforms) and feel at ease navigating technical systems.
Your Nalys Journey – Recruitment Process
First Conversation – Olivia Braszko, our Talent Acquisition Specialist at Nalys, reviews your application and contacts you for an initial discussion
Technical Interview – You meet with one of our technical leaders to explore your experience and expectations
Business Interview – A final exchange with, Jimmy Rousseaux, one of our Business Unit Directors to confirm the match and discuss future opportunities.
How to Apply
If you're excited about helping shape the digital future of pharmaceutical production, we'd love to hear from you
Apply directly on linkedin or contact your Talent Acquisition Specialist at Nalys.
Brussels area, Belgium
Introduction
At Nalys, we empower engineers to grow through exciting projects within leading life sciences environments. We are currently looking for a MES Design Engineer to support one of our pharmaceutical partners near Brussels.
In this role, you will contribute to the design, improvement, and maintenance of electronic Master Batch Records within a GMP‑regulated manufacturing context. If you are passionate about digitalizing production processes and ensuring high‑quality execution on the shop floor, this opportunity is for you.
Your Responsibilities
As an MES Design Engineer, you will be involved in activities such as:
Supporting the design and configuration of MES batch templates and production workflows
Translating process requirements into clear, compliant designs
Ensuring consistency, accuracy, and alignment with GMP and operational needs
Participating in the transposition and transformation of existing production documents into digital formats
Supporting updates, modifications, and improvements to existing MES recipes
Preparing and reviewing technical documentation, including rationales, change controls, and related quality documents
Working with engineering, production, QA, and validation teams to ensure smooth deployment of MES functionalities
Providing technical support during troubleshooting, testing, and qualification activities.
What You Bring
You hold a Bachelor's or Master's degree in Engineering, Life Sciences, IT, or a related field — or you've built equivalent technical expertise through hands‑on experience
You have at least one year of experience in the pharmaceutical or chemical industry, ideally in a role connected to digital manufacturing or production processes
You already have exposure to MES design, eMBR creation, or the digitalization of manufacturing workflows
You understand the fundamentals of GMP, validation practices, and process documentation
You are detail‑oriented, analytical, and comfortable collaborating with cross‑functional teams
You communicate fluently in English, and you can also work in French
You're confident using standard IT tools (Excel, Word, documentation platforms) and feel at ease navigating technical systems.
Your Nalys Journey – Recruitment Process
First Conversation – Olivia Braszko, our Talent Acquisition Specialist at Nalys, reviews your application and contacts you for an initial discussion
Technical Interview – You meet with one of our technical leaders to explore your experience and expectations
Business Interview – A final exchange with, Jimmy Rousseaux, one of our Business Unit Directors to confirm the match and discuss future opportunities.
How to Apply
If you're excited about helping shape the digital future of pharmaceutical production, we'd love to hear from you
Apply directly on linkedin or contact your Talent Acquisition Specialist at Nalys.
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