CSV Analyst
*CSV Analyst required by leading Pharmaceutical firm based in Dreux*
A global Pharmaceutical firm, based in Dreux, France, currently requires a CSV Analyst to be responsible for supporting the CSV team in delivering Global IT validation strategy and approach.
Upon joining, the CSV Analyst will act as a quality contact and subject matter expert for Computer Systems Validation (CSV) and Risk Management. The CSV Analyst will also be a main point of contact for the project teams in the assessment of new computerised systems or software for GxP impact.
In terms of skills, we are looking for CSV Analyst’s who have solid experience of working either as a CSV Analyst or working within a Quality/Validation team in the Pharmaceutical/Biotechnology or Medical Device industry.
A solid understanding of Regulatory requirement and QMS (Quality Management Systems) would also be good to have. Solid skills within both French and English would be preferred.
This opportunity would suit a current CSV Analyst who is looking to work in a global Pharmaceutical company or a Validation/Quality Engineer/Analyst who is looking to move in to a more CSV based role.
If this sounds exciting, please apply within to find out more.
Key Words: CSV, Computer Systems Validation, IT Validation, Risk, GxP, Quality, Validation, QMS, Quality Management Systems, Pharmaceutical, Biotechnology, Medical Devices, Dreux, France
- Agency: Cpl Life Sciences
- Reference: JO-2302-511420
Website: Cpl Life Sciences
- Posted: 28th February 2023
- Expires: 28th March 2023
