Quality Manufacturing Engineer - CI & CAPA Leader

Panda International

Groningen

Vor Ort

EUR 65.000 - 90.000

Vollzeit

vor 24 Stunden
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

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Zusammenfassung

Panda International in Groningen, Netherlands, seeks a Quality Manufacturing Engineer to oversee quality assurance activities at the factory, collaborating with Operations and Manufacturing Engineering to manage deviations, non-conformities, and escalations while ensuring procedural compliance and driving continuous improvement across manufacturing processes.

You will address non-conformities, guide planned deviations, review changes to production processes, analyze rejection data to reduce

Qualifikationen

  • Bachelor's degree in a relevant field.
  • 4–6 years of pharma or medical-device experience.
  • Fluent Dutch and English, written and spoken.
  • Detail-oriented, flexible and able to work independently or in a team.

Aufgaben

  • Address non-conformities in production and manage escalations.
  • Guide planned deviations from established production processes.
  • Review, advise on, and approve changes to production processes.
  • Analyse production rejection data to identify trends and reduce variation.
  • Identify improvements from performance trends and report to management.
  • Manage non-conformities and investigate CAPAs.
  • Drive continuous improvement in response to regulatory changes and data insights.
  • Write, review and support updating of operating procedures.

Kenntnisse

Dutch language
English language
Attention to detail
Independent worker

Ausbildung

Bachelor's degree or equivalent

Jobbeschreibung

Panda International in Groningen, Netherlands, seeks a Quality Manufacturing Engineer to oversee quality assurance activities at the factory, collaborating with Operations and Manufacturing Engineering to manage deviations, non-conformities, and escalations while ensuring procedural compliance and driving continuous improvement across manufacturing processes.

You will address non-conformities, guide planned deviations, review changes to production processes, analyze rejection data to reduce

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