ID oferty: 1443359
Źródło: adzuna
Kategoria: Unknown
Opis: You will lead planning, compilation and delivery of regulatory submission dossiers for lifecycle activities. You will coordinate with global submission teams, clinical, CMC (Chemistry, Manufacturing and Controls), quality, publishing and local regulatory partners. We value organised, collaborative people who communicate clearly and focus on practical solutions. This role offers visible impact on patient access, clear growth opportunities, and aligns with GSK’s mission of uniting science, techno…
Wynagrodzenie min: 1.584e+06
Wynagrodzenie max: 2.64e+06
Utworzono: 24.09.2026 18:59