Senior Qa Manager, Quality Systems, Temporary Position

Zealand Pharma AS

Copenhagen, Denmark
Onsite
5+ years qa experience in pharmaceutical development
Expertise in qmr, deviations, and capa processes
Experience with veeva vault electronic qms
Zealand Pharma is seeking a Senior QA Manager for a temporary 12-month position focused on enhancing its Quality Management System (QMS) within the pharmaceutical development sector. The ideal candidate will possess a strong background in QA processes, data analysis, and collaborative communication to drive improvements and support decision-making

Job Summary

  • This temporary 12-month role focuses on driving continuous improvement in the Quality Management System across pharmaceutical development.
  • The successful candidate will own core QA processes including Change Control, Deviation management, and Quality Management Reviews while ensuring compliant ways of working.
  • You will collaborate closely with stakeholders to structure, analyze, and report quality data using tools like Veeva Vault and BI platforms to support decision-making.

Matching Summary

Match Score: 85

Zealand Pharma is seeking a Senior QA Manager for a temporary 12-month position focused on enhancing its Quality Management System (QMS) within the pharmaceutical development sector. The ideal candidate will possess a strong background in QA processes, data analysis, and collaborative communication to drive improvements and support decision-making.

Skills & Requirements

Must-have

  • 5+ years QA experience in pharmaceutical development
  • Expertise in QMR, Deviations, and CAPA processes
  • Experience with Veeva Vault electronic QMS
  • Ability to build KPI dashboards and trend analyses
  • Strong communication for audits and inspections

Nice-to-have

  • Pragmatic and data-oriented mindset
  • Collaborative team player with quality-first approach
  • Experience translating complex data into actionable insights

Key Requirements

  • Master's degree in a relevant field
  • 5+ years of QA experience
  • Solid understanding of pharmaceutical quality systems

Work Rights

Not specified

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