Alternance - Affaires Réglementaires (h/f) – 12 Mois
GlaxoSmithKline
Master ii in pharmacy or regulatory affairs
Current intern status in pharmacy
Fluent english proficiency
The role involves analyzing, preparing, and tracking marketing authorization dossiers and clinical variations for national and European procedures
Job Summary
The role involves analyzing, preparing, and tracking marketing authorization dossiers and clinical variations for national and European procedures.
Candidates will manage product information updates, control packaging compliance, and participate in regulatory compliance activities such as CAPA and quality reviews.
This is a 12-month internship within a team of 13 at GlaxoSmithKline, offering interaction with internal departments and external teams across multiple therapeutic areas.
Matching Summary
The role involves analyzing, preparing, and tracking marketing authorization dossiers and clinical variations for national and European procedures.
Skills & Requirements
Must-have
Master II in Pharmacy or Regulatory Affairs
Current intern status in pharmacy
Fluent English proficiency
Strong organizational and analytical skills
Interest in pharmaceutical regulation
Nice-to-have
Teamwork and collaborative spirit
Proactive initiative and relationship building
Experience with therapeutic areas like oncology
Ability to synthesize complex information
Key Requirements
Master II degree in progress
Internship in pharmacy required
Specialization in industry or health law preferred