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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