V.I.E. Quality Assurance Engineer

Job description

Description du poste

About the Quality Assurance Coordinator position:

As a Quality Assurance consultant in the pharmaceutical industry, you will be working in our partners’ QA departments as the guarantor of the quality policy and objectives defined in accordance with GMP.

Your responsibilities will include

Drawing up risk analyses;
Participating in the investigation of deviations;
Carry out internal audits;
Ensure the correct implementation and monitoring of CAPA’s;
Review and approve documents relating to operations (SOPs, teaching tools, batches, reports and other GMP-related documents);
Contribute to improving the content and process of the quality system;
Develop solutions to reduce quality-related risks;
Assessing changes as part of change control.

Qualifications

Your profile:

Master’s degree in Bio-Engineering, Industrial Pharmacy or related fields.
You have experience of quality systems (non-conformity, compliance, etc.) and GMPs.
You have knowledge of the production process and QA in the pharmaceutical industry
You are able to work in English as well as French

Informations supplémentaires

What are the advantages of a V.I.E?  

Gain professional experience abroad with the support of Business France and ALTEN. 

Improve your language skills 

Find an environment where you can express yourself fully 

Benefit from tax-free pay  

Discover a new city and new cultures.