Regulatory Affairs Specialist at lfb

This Regulatory Affairs role manages clinical-regulatory strategy and execution across product development, clinical study approvals, health-authority consultations, marketing authorization submissions and lifecycle management, regulatory compliance, pharmacovigilance documentation, and global product labelling. The position requires a scientific or quality-focused master's degree, a PhD in Pharmacy, or a master's in Regulatory Affairs, with at least one year of Regulatory Affairs experience for the latter qualification. It is offered as a permanent contract, with hybrid telework available after four months of seniority and several health and workplace benefits.