Alternance En Compliance Pharmaceutique / Réglementaire Site H/f
GlaxoSmithKline
Evreux, France
Regulatory impact assessment
Maintain marketing authorisation dossiers
Regulatory intelligence
Within the Regulatory Quality team, you will primarily assess regulatory impacts according to the guidelines of major markets and ensure the maintenance of Marketing Authorisation Dossiers
Job Summary
Within the Regulatory Quality team, you will primarily assess regulatory impacts according to the guidelines of major markets and ensure the maintenance of Marketing Authorisation Dossiers.
You will be responsible for regulatory watch and compliance with applicable regulations across different markets, as well as proposing and participating in continuous improvement actions.
The Evreux site is a major player in the manufacturing of respiratory medications and is one of GSK's 3 largest industrial sites, contributing significantly to the company's global turnover.
Matching Summary
Within the Regulatory Quality team, you will primarily assess regulatory impacts according to the guidelines of major markets and ensure the maintenance of Marketing Authorisation Dossiers.
Skills & Requirements
Must-have
Regulatory impact assessment
Maintain Marketing Authorisation Dossiers
Regulatory intelligence
Regulatory compliance monitoring
Continuous improvement initiatives
Nice-to-have
Methodology and curiosity
Team collaboration
Proactive communication
Key Requirements
Ingénieur / Pharmacien with Master's in Regulatory Affairs