Reporting to the Head of Pharmaceutical Affairs, and working closely with the Quality/Regulatory Affairs Managers, you will assist the Pharmaceutical Affairs Department with all Regulatory Affairs projects and certain Quality Assurance activities, for all the Group’s brands. 

Missions: Be the day-to-day operational support for: 

– Creating and updating product regulatory files,

– Guaranteeing the conformity of technical documents relating in particular to raw materials or packaging items, 

– Completing and updating work databases, 

– Participating in the implementation of PLM (Product Lifecycle Management) software, 

– Preparation of export registration files, 

– Creating technical documents related to supplier specifications.

Profile: In higher scientific education (Bac+4 to Bac+5), you would like to acquire skills in Regulatory Affairs in a cross-disciplinary, multi-skilled position. 

We offer you the opportunity to integrate into a dynamic laboratory, in a department at the interface with all other departments (R&D, marketing, purchasing). 

A knowledge of cosmetic regulations and/or food supplements would be a major asset. 

Quality requirements: Rigorous and organised, you are proactive, autonomous and able to meet deadlines and comply with procedures. 

You have good interpersonal skills and enjoy working in a team. You know how to manage priorities, take the initiative and have good analytical and summarising skills. 

Working English (technical English, reading and writing) and knowledge of office tools (Word, Excel, PPT, etc.) are essential.. 

Laboratoire NOREVA – Clermont-Ferrand

Anne-Céline MINVIELLE, Head of Pharmaceutical Affairs

ac.minvielle@noreva.com