Quality Control

Senior Quality Advisor – 11871

Gothenburg, Sweden
Onsite

Huy Tran

HR Administrator

cv@veritaz.se

Job Summary

  • Posted Date

    March 7, 2025

  • Work Type

    Onsite

  • Deadline

    2025-03-10

  • Schedule

    Full-time

  • Location

    Gothenburg, Sweden

Job Description

Assignment Description:

We are looking for a Senior Quality Advisor to join our dynamic team.

What you will work on:

  • Responsible for quality release of manufactured Drug Product and Investigational Medicinal Product for clinical trials.
  • Support pharmaceutical development functions with investigations of deviations, changes, and other quality and compliance decisions related to drug product.
  • Provide proactive quality advice to support the development, implementation, and continuous improvement of GMP quality systems across Clinical Supply functions.
  • Operate as part of a global organisation with an integrated mindset, creating common processes and ways of working.

What you bring:

  • MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years’ experience within a pharmaceutical GMP environment.
  • Understanding of international quality systems regulations, concepts, and industry practices to adopt best-in-class processes.
  • Comprehensive understanding of GMP regulations, the pharmaceutical development process, and supply chain processes is advantageous.
  • Experience in effective cross-interface collaboration.
  • Fluent in written and spoken English.

If this sounds interesting, please send your CV to cv@veritaz.se

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