Pharma Project Engineer: Quality, Validation & Compliance

Project Engineer - (GxP Environment); Diegem; Vor Ort; EUR 60.000 - 90.000; Vollzeit

Benefits dieser Stelle

Mobility options (incl. company car)

Insurance coverage

Meal vouchers

Eco-cheques

Sopra Steria Academy

Team events

Zusammenfassung

Sopra Steria is seeking a Project Engineer to ensure GxP systems meet regulatory requirements throughout the lifecycle. You will drive specification, procurement, installation, validation and handover, while coordinating with multidisciplinary teams and suppliers.

A strong focus on quality, compliance and continuous improvement is required. Ideal candidates hold a Master’s degree in engineering or science and have GMP experience, with excellent organizational and communication skills.

Qualifikationen

• Master’s degree in a technical or scientific field.
• Experience in pharmaceutical and/or GMP environment is a strong asset.
• Knowledge of validation processes and sterile production is a plus.
• Strong organizational and communication skills.
• Ability to work independently and take initiative.
• Team player with analytical thinking skills.
• Flexibility and resilience in dynamic projects.
• Experience in project coordination and contractor management is a plus.
• Proficiency in English; Dutch is a plus.

Aufgaben

• Oversee the full project lifecycle: from specification and procurement to installation, validation and handover to operations.
• Collaborate in multidisciplinary teams and monitor planning and budget.
• Ensure safe, compliant and efficient execution and quality throughout.
• Provide technical follow-up with suppliers and communicate with stakeholders.

Kenntnisse

Organizational skills

Communication skills

Initiative

Team player

Analytical thinking

Ausbildung

Master’s degree in engineering or science

Jobbeschreibung

Sopra Steria is seeking a Project Engineer to ensure GxP systems meet regulatory requirements throughout the lifecycle. You will drive specification, procurement, installation, validation and handover, while coordinating with multidisciplinary teams and suppliers.

A strong focus on quality, compliance and continuous improvement is required. Ideal candidates hold a Master’s degree in engineering or science and have GMP experience, with excellent organizational and communication skills.