We assist our clients through non-clinical and clinical studies to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences.
For each customer and each project, we design customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs.

You will report to the Director Compliance

You will be part of a team of 8 persons

In this role, you will be accountable for
• Managing Standard Operating Procedures
• Training personnel in procedures and the Quality System
• Maintaining and developing the Quality System
• Updating the Site Master File
• Monitoring Key Quality Indicators and Key Performance Indicators
• Promoting risk management and continuous improvement strategies
• Drawing up the Quality Management Review (QMR)
• Managing CAPAs
• Carrying out and following up client and regulatory agency audits
• Carrying out internal audits of facilities, processes and projects
• Assessing quality contracts provided by clients
• Monitoring quality in client projects
• Advising clients on subjects related to quality
• Qualifying providers

• Scientific background
• Relevant experience in a similar role in the pharmaceutical industry
o Good knowledge of the pharmaceutical sector, Quality Assurance
principles, GMP and ICH guidelines
• Very good communication and writing skills both in French and English
(contacts with clients, authorities, Audit management)
• At ease with office IT tools

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