Are you ready to shape regulatory strategies that bring life-changing medicines to the patients who need them most? Join a team where your expertise in regulatory affairs and pharmacovigilance directly safeguards our licence to operate – and protects the safety of millions of people living with serious chronic diseases.

Your new role

As a Regulatory Affairs & Pharmacovigilance (RAPV) Associate, you will play a pivotal role in ensuring regulatory compliance and driving pharmacovigilance activities across our portfolio. You will monitor the regulatory environment, coordinate submissions and provide expert insight to stakeholders shaping the future of our products in the market.

Day-to-day your tasks will include: