Consultant Pharmacien Assurance Qualité H/F

NEW

Offer details

Consultant Pharmacien Assurance Qualité H/F
Rouen - France
Permanent
Pharmaceutical Industry
Work in progress - accepting candidates
5 days
Service provision

Wanted profile

Experience level
10+ years
Level of education
Master's Degree
Mandatory working languages
English,French
Skills
Gmp Quality assurance product Quality assurance system
+ 5 skills

Your Profile:

  • You have obtained a Pharmacist - Doctor of Pharmacy diploma, registered in section B.
  • You have at least 5 years' experience in Pharmaceutical Quality Assurance
  • You are familiar with the specific requirements of the pharmaceutical/medical device/biotech industry
  • You have the communication skills needed for cross-functional work
  • Operational English you are able to work in an English-speaking professional environment


Context

At Anywr.Life - we specialise in Life Sciences, and can take care of your mobility project from A to Z, whether in France or abroad.


Our specialists in the life sciences sector are here to help you:

Finding your future job? Changing region? Finding your future home? Enrolling your children at school? Saying goodbye to administrative hassles? It's easy with ANYWR, we're experts in these matters!


To join our Life Sciences Consulting team in France, we are now recruiting a Pharmaceutical Quality Assurance Consultant.


Job offer CDI Anywr France



Mission

Your main task will be to provide technical and management solutions for our customers in the pharmaceutical industry to improve the performance and quality of their environment.


You will work directly on our partners' sites in a GMP environment, in project mode.


Your role as a Quality Assurance Pharmacist consultant will be to contribute to our customers' projects such as :

  • Managing all the Quality Assurance processes in a pharmaceutical production laboratory (dry forms, injectables, vaccines)
  • Ensure product quality review (PQR)
  • Review and improve the quality system
  • Participate in the creation and validation of major documents such as plans and validation reports
  • Review and release batch files
  • Analysing discrepancies and updating CAPAs, corrective and preventive actions, deviations, anomalies and root cause analyses


Apply

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