Project Engineer - (GxP Environment) M/V/X

WERAANBIEDING UIT EEN ANDERE REGIO

Diegem

In loco

EUR 60.000 - 90.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Descrizione del lavoro

Sopra Steria is seeking a highly motivated professional to join our pharma and life sciences projects in Belgium. You will contribute to digital transformation and technology consulting in a GMP environment, applying validated processes and sterile production knowledge to deliver compliant solutions.

The role requires a Master's degree in a technical field, strong organizational and communication skills, and the ability to work independently within dynamic projects.

Competenze

  • Master's degree in a technical or scientific field (industrial, civil, or bio-engineering).
  • Experience in a 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.
  • Affinity with technical, technological, and process-related aspects.
  • Flexible and resilient in a dynamic project environment.
  • Experience in project coordination and contractor management is a plus.
  • Good command of English is required and Dutch is a plus.

Conoscenze

Pharma/GMP experience
Validation processes

Formazione

Master's degree in technical/scientific field (industrial, civil or bio-engineering)

Descrizione del lavoro

We're seeking passionate colleagues who are eager to push the boundaries in digital transformation and technology consulting. At Sopra Steria, you'll have the opportunity to grow your skills in a constructive, collaborative team environment, working on impactful projects that drive change for our clients. If you thrive on challenge and meet (most of) the qualifications below, we look forward to your application!

  • Master's degree in a technical or scientific field (industrial, civil, or bio-engineering)
  • Experience in a 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
  • Affinity with technical, technological, and process-related aspects
  • Flexible and resilient in a dynamic project environment
  • Experience in project coordination and contractor management is a plus
  • Good command of English is required and Dutch is a plus
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