Zentiva Group is seeking a Regulatory Lead to oversee and organize a team responsible for the registration of medicinal products, ensuring compliance with regulatory requirements. The ideal candidate will have several years of experience in a pharmaceutical regulatory role, strong organizational skills, and fluency in English
Job Summary
The role involves leading and organizing the pharmaceutical registration team while planning tasks and priorities.
Candidates will manage full lifecycle registration, re-registration, and post-marketing changes for medicinal products in Poland and the EU.
The company offers attractive employment conditions, professional development opportunities, and a great working atmosphere.
Matching Summary
Match Score: 85
Zentiva Group is seeking a Regulatory Lead to oversee and organize a team responsible for the registration of medicinal products, ensuring compliance with regulatory requirements. The ideal candidate will have several years of experience in a pharmaceutical regulatory role, strong organizational skills, and fluency in English.
Skills & Requirements
Must-have
Leading registration team operations
Managing drug product registration processes
Ensuring compliance with Polish and EU laws
Nice-to-have
Strong organizational and prioritization skills
Ability to work under time pressure
Excellent English communication skills
Key Requirements
Higher education in medical sciences, pharmacy, or biotechnology
Several years of managerial experience in pharmaceutical registration
Knowledge of pharmaceutical law and registration procedures