Ema Vacatures In Veendam, Groningen - 2 Job Positions Available

About the Opportunity We are seeking a Regulatory Affairs professional to join a growing pharmaceutical consultancy supporting innovative biotech and pharmaceutical clients across Europe. This position offers exposure to a broad range of regulatory activities spanning

Deputy QP Overall Job Purpose: The Senior Qualified Person (QP) will be responsible for certifying the release of IMPs for clinical trials in compliance with European and international GMP (Good Manufacturing Practice) standards. This role is