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Compliance and Quality professional - part time

Do you want to be the expert we all ask for advice, and who ensures that our quality assurance system is in compliance with applicable regulations for medicinal products and medical devices?

Further develop and maintain the right quality level
In this role you will be responsible for improving and maintaining the right quality level at Azanta A/S. You will cover all areas of Azanta and collaborate with our warehouse staff, regulatory affairs, sales & marketing, affiliates as well as CROs and CMOs.

We expect you to independently handle change control cases, SOPs, Quality Management Review and complaints, as well as participate in audits and Health Authority inspections. You will also continuously support issues regarding compliance and quality within all aspects of the business. In addition, we hope that you have the opportunity to assist Medical Affairs and Regulatory Affairs in busy times. In the position, you will refer to the Director of Regulatory Affairs and QA.

Quality mindset and good cooperative skills
We imagine that you have at least 2-3 years of experience from a GxP/QA organization or associated quality systems, perhaps from a previous QA role or from production. You are a pharmacist or have other relevant background qualifying you as a delegated QP. You can translate the GMP rules and facilitate their implementation in our daily lives communicating them in both Danish and English. Your personal skills make you act proactively, be analytical and structured, still with a pragmatic approach. You have a natural sense of curiosity, you are good at creating relationships with your colleagues and collaborators and finally you have a good sense of humor.

We offer
A 30 hour a week position with many opportunities within QA and related areas. Competitive compensation package in an exciting growing international company. You will have a very busy, diverse and exciting work day which you will largely be able to plan yourself.

Application deadline and information
For further information, please contact Nete Søgaard Poulsen, Director RA&QA on +45 5239 9890. We need your application no later than 11 December 2017 to

Azanta A/S, Gearhalsvej 1, DK-2500 Valby, Denmark, Phone +45 7025 9545, Fax: +45 7025 9546, Mail:

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