Quality Assurance Officer – GMP/GxP for Biotech Scale-Up

Citryll

Netherlands

Remote

EUR 60.000 - 80.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Citryll is seeking a QA Officer to support the implementation, maintenance and execution of the Quality Management System (QMS) to ensure quality and regulatory compliance across product development, manufacturing and testing.

You will work with the QA Manager and cross-functional teams to apply GMP/GLP/GCP standards, manage deviations, CAPAs, and supplier quality oversight as the company scales.

Qualifikationen

  • Bachelor’s degree in a relevant scientific or quality discipline.
  • 2–5 years QA experience in pharma/biotech.
  • GMP/GLP/GCP knowledge and regulatory familiarity.

Aufgaben

  • Ensure GxP compliance across internal R&D and external partners (CDMOs, CROs, testing labs) supporting development, manufacturing, and clinical activities.
  • Maintain and develop the Quality Management System (QMS) including document control, SOPs, records, and training compliance.
  • Manage deviations, CAPAs, and change control across both internal activities and outsourced operations, including investigations and effectiveness checks.
  • Provide quality oversight of external suppliers including qualification, quality agreements, audit support, and issue follow-up.
  • Partner with R&D, clinical, CMC, and external vendors to ensure quality and regulatory expectations are built into development programs.

Kenntnisse

Attention to detail
Structured approach
English communication
Cross-functional teamwork
Proactive mindset

Ausbildung

Bachelor’s degree in scientific/quality field

Jobbeschreibung

Citryll is seeking a QA Officer to support the implementation, maintenance and execution of the Quality Management System (QMS) to ensure quality and regulatory compliance across product development, manufacturing and testing.

You will work with the QA Manager and cross-functional teams to apply GMP/GLP/GCP standards, manage deviations, CAPAs, and supplier quality oversight as the company scales.

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