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You will be updated with latest job alerts via emailAbout 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 CAPAs;
Review and approve documents relating to operations (SOPs teaching tools batches reports and other GMPrelated documents);
Contribute to improving the content and process of the quality system;
Develop solutions to reduce qualityrelated risks;
Assessing changes as part of change control.
Qualifications :
Your profile:
Masters degree in BioEngineering Industrial Pharmacy or related fields.
You have experience of quality systems (nonconformity 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 supplmentaires :
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 taxfree pay
Discover a new city and new cultures.
Remote Work :
No
Employment Type :
Fulltime
Full-time