Lead Engineer, Fill & Finish Systems & Automation

Prothya Biosolutions (operating under Accord Plasma B.V. / Intas Pharmaceuticals); Brussel Hoofdstad; Presencial; EUR 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Meal vouchers

Eco-cheques

Flex Reward Plan

Holiday entitlement beyond legal

Homeworking after onboarding

Descripción de la vacante

Prothya Biosolutions Belgium is seeking a Lead Engineer for Fill & Finish in Brussels to act as a system architect for multiple application domains and as technical owner of several systems. You will support the engineering team as SME and lead cross-department projects to implement roadmaps and improvements.

The role requires a Master in engineering, 8 years total experience including 3 years in pharma, strong GMP/GEP knowledge, and proactivity in a collaborative environment.

Formación

• Master in engineering technology (ING) or Master of engineering science (IR) or equivalent
• Preferably 3 years in a similar pharma role; total 8 years of professional experience

Responsabilidades

• System architect for one or more application domains (equipment/utilities/automation)
• Technical system owner for several systems throughout their lifecycle
• Provide SME support and guidance to other engineers
• Lead and manage cross-domain projects to implement roadmaps

Conocimientos

Domain knowledge

GMP/GEP knowledge

Analytical thinking

English + Dutch/French

Problem solving

Team collaboration

Proactivity

Educación

Master in engineering (ING) or Master of engineering science (IR)

Herramientas

MS Office

MS Project

Descripción del empleo

Prothya Biosolutions Belgium is seeking a Lead Engineer for Fill & Finish in Brussels to act as a system architect for multiple application domains and as technical owner of several systems. You will support the engineering team as SME and lead cross-department projects to implement roadmaps and improvements.

The role requires a Master in engineering, 8 years total experience including 3 years in pharma, strong GMP/GEP knowledge, and proactivity in a collaborative environment.