Hobson Prior are currently looking for a Senior Expert CQV to join a brilliant consultancy on a permanent basis located in Toulouse. Our client is focused on improving people's health through the distribution of regulatory compliance services.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this role, you will be responsible for approving risk analysis linked to the modifications as well as of qualification protocols such as DQ/IQ/OQ/PQ etc.
• Agree on qualification reports affiliated with the protocols.
• Manage the approval of both cleaning validation and periodic validation evaluations.
• Contribute to the production or update of changeover protocols to identical/correspondent.
• Partake in the drafting of the PPR for the technical QA/central validation part.
• Endorse the production or update of documents linked to qualification, such as traceability matrix, etc.
• Any other assigned duties.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.