MES Business Analyst: Digital Transformation Life Sciences

Mantu Manager Program; Brussel; Sur place; EUR 55 000 - 85 000; Plein temps

Résumé du poste

Amaris Consulting in Brussels is seeking a motivated MES Business Analyst to bridge business needs and MES solutions in a regulated life sciences environment. You will collaborate with production and IT teams to support digital transformation and ensure compliant MES implementations.

The role requires analyzing requirements, translating them into functional specs, participating in validation and testing, and driving continuous improvement within GMP/CSV frameworks.

Qualifications

• Master’s degree in Engineering, IT, Life Sciences, or a related field.
• Minimum 3 years of experience as a Business Analyst or MES Functional Consultant.
• Experience in the pharmaceutical or life sciences industry is a strong plus.
• Fluent in French and English.
• Knowledge of MES systems and manufacturing processes in regulated environments.
• GxP and Computer System Validation (CSV) knowledge.
• Willingness to be based in Brussels with mobility.

Responsabilités

• Gather, analyze, and formalize business requirements from manufacturing and quality stakeholders.
• Translate business needs into functional specifications for MES solutions.
• Support the implementation and enhancement of MES systems (production execution, batch tracking, electronic batch records).
• Collaborate with IT teams, production teams, and quality assurance to ensure system alignment.
• Participate in validation activities and ensure compliance with GxP and CSV standards.
• Support testing phases (FAT, SAT, UAT) and ensure proper documentation.
• Contribute to continuous improvement of manufacturing processes through digital solutions.

Connaissances

Analytical mindset

Communication skills

French and English fluency

Formation

Master’s degree in Engineering/IT/Life Sciences

Description du poste

Amaris Consulting in Brussels is seeking a motivated MES Business Analyst to bridge business needs and MES solutions in a regulated life sciences environment. You will collaborate with production and IT teams to support digital transformation and ensure compliant MES implementations.

The role requires analyzing requirements, translating them into functional specs, participating in validation and testing, and driving continuous improvement within GMP/CSV frameworks.