Manufacturing Engineer

X4 Life Sciences; Antwerpen; Hybride; EUR 70 000 - 100 000; Plein temps

Avantages offerts par ce poste

Hybrid working model

Exposure to multiple clients

Résumé du poste

X4 Life Sciences in Belgium is seeking an MES Consultant to join a growing Life Sciences practice. You will design, implement and deliver MES solutions for pharmaceutical and biotech clients, focusing on PAS‑X or similar platforms and working across client sites.

The role requires hands-on MES experience in regulated environments, strong problem-solving, and excellent stakeholder communication. A hybrid working model and exposure to multiple projects offer clear career progression.

Qualifications

• 2+ years’ hands-on experience with MES
• Hands-on MES implementation experience
• Experience with MBR modelling / recipe design would be beneficial
• Experience in a regulated manufacturing environment is essential
• Strong communication and stakeholder-management skills
• Fluent English and client-facing consulting experience
• Willingness to learn and adapt across client environments

Responsabilités

• Designing and configuring MES solutions for life sciences clients
• Conducting MBR modelling and recipe design activities
• Supporting MES implementation, testing, deployment and go-live
• Collaborating with client stakeholders and manufacturing users
• Assisting requirements gathering and design workshops
• Translating manufacturing requirements into MES solutions
• Supporting validation/verification activities, including MBR/EBR verification
• Troubleshooting MES-related issues and driving continuous improvement
• Collaborating with IT, Engineering, QA, Validation and Manufacturing teams
• Contributing to projects from requirements through implementation and support

Connaissances

MES experience

Client-facing

Regulated environment

Problem-solving

English fluency

Stakeholder management

Manufacturing processes

Willingness to learn

Communication skills

Description du poste

Manufacturing Execution System (MES) Consultant – Life Sciences

Location: Belgium

Working Pattern: Hybrid – typically 3 days per week on client site

Type: Permanent

Shape the Future of Digital Manufacturing in Life Sciences

Are you an experienced MES professional looking to develop your career within a leading consulting environment? I am supporting the expansion of a specialist Life Sciences MES team in Belgium, working with leading pharmaceutical and biotech organisations on digital manufacturing and MES transformation projects.

We are looking for consultants with hands‑on MES implementation experience who are comfortable working in regulated manufacturing environments and are passionate about technology, problem‑solving and continuous improvement.

Pharmaceutical experience is a major advantage, particularly experience working with MES within GMP‑regulated manufacturing environments.

The team works across multiple client sites and projects in Belgium, with opportunities to gain exposure to different manufacturing environments, technologies and challenges.

Experience with Werum PAS‑X is particularly relevant, alongside other life sciences MES platforms.

Your Role

As an MES Consultant, you will contribute to the design, implementation and delivery of MES solutions for pharmaceutical and life sciences clients.

Depending on your experience and the project, responsibilities may include:

• Designing and configuring MES solutions within life sciences manufacturing environments
• Performing MBR (Master Batch Record) modelling and recipe design
• Supporting MES implementation, testing, deployment and go‑live activities
• Working directly with client stakeholders and manufacturing users
• Supporting requirements gathering and design workshops
• Translating manufacturing requirements into effective MES solutions
• Supporting validation and verification activities, including MBR and EBR verification
• Troubleshooting MES‑related issues and supporting continuous improvement
• Collaborating with IT, Engineering, QA, Validation and Manufacturing teams
• Contributing to projects from initial requirements through to implementation and ongoing support

The role offers the opportunity to work across different client environments, so adaptability and the ability to quickly understand new processes and technologies are important.

What We’re Looking For

Essential

• 2+ years’ hands‑on experience working with MES
• Practical experience with MES implementation
• Hands‑on MBR modelling / recipe design experience
• Strong understanding of manufacturing processes
• Experience working within a regulated manufacturing environment
• Strong communication and stakeholder‑management skills
• Fluent English
• Comfortable working in a client‑facing consulting environment
• Strong problem‑solving and analytical skills
• Willingness to learn and adapt to different client environments

Pharmaceutical / Life Sciences Experience

Pharmaceutical or biotech manufacturing experience is a strong advantage.

Experience working within GMP / GxP environments and an understanding of validation, data integrity and regulated manufacturing processes would be highly beneficial.

Desirable

• Werum PAS‑X experience
• Experience with other life sciences MES platforms such as PharmaSuite or similar
• MBR / EBR verification experience
• MES installation or technical infrastructure experience
• CSV / validation experience
• Experience integrating MES with ERP, automation or other manufacturing systems
• Previous consulting experience
• Dutch, Flemish and/or French language skills

Who You Are

You are technically strong but also enjoy working with people.

You can understand a client's manufacturing challenge, ask the right questions and translate business requirements into practical technical solutions.

You are comfortable working with different stakeholders and can adapt your communication depending on whether you are speaking with a manufacturing operator, technical specialist, QA professional, IT team or senior client stakeholder.

You don't need to know every technology already. A willingness to learn and the ability to approach unfamiliar problems logically are equally important.

Whether you currently work in MES consulting or directly within a pharmaceutical / biotech manufacturing organisation, we would be interested in speaking with you if you have genuine hands‑on MES implementation experience.

What You Can Expect

• Permanent career opportunity within a leading consulting organisation
• Work on major Life Sciences digital manufacturing programmes
• Exposure to multiple clients and manufacturing environments
• Opportunity to work with PAS‑X and other leading MES technologies
• Structured professional development and continuous learning
• Collaboration with experienced MES and Life Sciences specialists
• Opportunities to develop both technical and client‑facing consulting skills
• Potential for progression into senior technical, project or consulting responsibilities
• Hybrid working model

Location & Travel

The role is based across client sites in Belgium.

You should expect to be on client site approximately 3 days per week, depending on the requirements of your project.

Projects may involve travel to different locations across Belgium, with additional travel possible depending on client and project requirements.

Flexibility around travel and working across different client environments is therefore important.

Why This Opportunity?

This is an opportunity to move beyond working on a single MES environment and develop your career within a specialist consulting team.

You will have the opportunity to:

• Work with multiple Life Sciences clients
• Gain exposure to different MES implementations
• Develop your PAS‑X / MES expertise
• Build stronger client‑facing and consulting skills
• Work on complex digital manufacturing programmes
• Learn from experienced industry specialists
• Progress your career within a growing consulting environment