Step into a dynamic Regulatory Affairs Lead role where you’ll own regulatory delivery, accelerate approvals through proactive strategy, and grow your impact across cross‑functional and external stakeholder networks.

 

Your new role
As Regulatory Affairs Lead for Levant, you will own regulatory strategy and safety oversight for assigned products and projects. You will lead regulatory submissions and approvals- prepare, , product registrations and amendments, and respond to health authority queries.

 

Day‑to‑day you will:

 

Ensure compliance and governance- maintain adherence to global and local regulatory standards, conduct reviews and audits, and manage compliance risks. Oversee pharmacovigilance activities: supervise collection, analysis and reporting of safety data, identify new safety signals and ensure timely regulatory reporting. Collaborate with stakeholders, partner with clinical, safety, commercial and external partners, and act as the company’s regulatory and safety contact for health authorities and policymakers. Monitor regulatory trends and adapt strategy, track regulatory changes, assess impact, and develop approaches to maintain compliance and accelerate approvals.

 

Your new department
You will be part of the Regulatory Affairs & Safety Pharmacovigilance function within CMR Levant. The department works cross‑functionally to enable, product launches and market access while ensuring high standards of patient safety and regulatory compliance.

 

Your skills & qualifications

To succeed in this role you should bring:

 

Bachelor degree as a minimum in a life science or medical discipline (e.g., MD, PharmD. Pharmacy) 5–7+ years’ experience in regulatory affairs within the multinational pharmaceutical industry. Proven track record managing regulatory submissions, compliance activities and safety data analysis. Experience engaging with health authorities and leading cross‑functional regulatory or safety initiatives. Strong knowledge of global and local regulatory frameworks. Excellent attention to detail, problem‑solving skills, and the ability to communicate complex regulatory and safety information clearly. Proficiency in English (written and spoken); 

 

As a professional, you are strategically minded, resilient and adaptable, with strong stakeholder collaboration skills and the ability to make independent decisions. You combine regulatory expertise with a patient‑safety focus and the capability to influence cross‑functional teams.

 

Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

 

What we offer
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

 

Deadline 
22nd of February. (Applications are reviewed on an ongoing basis)

 

 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

 

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.