Pharma Validation & Compliance Project Engineer — Hybrid

Capgemini; Diegem; Hybride; EUR 52 000 - 76 000; Plein temps

Avantages offerts par ce poste

Hybrid working

Mentoring programs

Free learning platforms

Résumé du poste

Capgemini Engineering in Flanders, Belgium, seeks a Medior Project Engineer - Validation & Compliance to coordinate validation and verification activities within capital projects in a regulated pharmaceutical environment. You will act as the interface between Engineering and Quality Assurance to ensure safe, compliant project delivery.

You will apply GMP, ISO and ICH standards, draft validation protocols, support QRM, manage multiple projects, and contribute to process improvements.

Qualifications

• Master's degree in Engineering or a relevant scientific field.
• At least 2 years' experience in a regulated pharmaceutical or production environment.
• Fluent in Dutch and English with strong technical writing capabilities.
• Experience with aseptic processes, cleaning, disinfection, sterilisation is a plus.

Responsabilités

• Coordinate validation and verification activities across capital projects.
• Interpret GMP, ISO and ICH standards and liaise with QA for compliant delivery.
• Draft, review and manage validation protocols and qualification docs.
• Support Quality Risk Assessments and investigations; manage multiple projects.
• Provide backup support to fellow project engineers as needed.

Connaissances

Communication

Stakeholder management

Cross-functional collaboration

Technical writing

Project coordination

Attention to detail

Formation

Master's degree in Engineering / related field

Description du poste

Capgemini Engineering in Flanders, Belgium, seeks a Medior Project Engineer - Validation & Compliance to coordinate validation and verification activities within capital projects in a regulated pharmaceutical environment. You will act as the interface between Engineering and Quality Assurance to ensure safe, compliant project delivery.

You will apply GMP, ISO and ICH standards, draft validation protocols, support QRM, manage multiple projects, and contribute to process improvements.