Project Manager for Pharma Software, French Speaking

We have an exclusive opportunity available to work with a global leader in providing regulatory affairs operating systems to the pharmaceutical and medical device industries. French speaking to an advanced level is essential for this role as our client intends for the role to be focused on working with their French speaking clients.

This is a unique opportunity to utilise broad managerial responsibilities throughout the software installation process and to be an expert in GxP/GAMPV/EMA/FDA validated environments to ensure that the regulatory affairs system is installed effectively for top 20 pharmaceutical, biopharmaceutical and medical device companies. A typical installation of a Regulatory Affairs Information Management system (RIMS) may take 1-3 years, our client provides their solutions via a cloud/SaaS based solution.

There is a minimum requirement of 1 year experience working specifically as Project Manager for installing life science software systems. PMP/PIP or Prince II qualification and experience in working with GAMP is preferred. Prior working experience of MDM, Master Data Management is nice to have. French speaking is essential. The role is on a full time, permanent basis and pays a competitive annual salary plus quarterly bonus.

I hope that the role will be of interest to you, there is a detailed job description available on request, I understand that you may require further information before applying to the client however please feel free to apply via this website and I will answer any questions you have. I am also available for phone calls at anytime to further discuss.

Kind regards,

Michael Kellitt

Job Code: 102918

Key words: chef de projet, pharmaceutique, logiciel, RA, Regulatory Affairs Operation, Regulatory Affairs Operations, Regulatory Affairs System, Regulatory Affairs Project Manager, Regulatory Affairs Systems Manager, RIMS