Regulatory Affairs Professional
Job Summary
Do you thrive on managing the product lifecycle Does being responsible for submission documentation excite you Can you deliver quality under strict deadlines If you answered yes then this role maybe for you. Your regulatory expertise will directly shape how our treatments reach patients faster navigating complex landscapes so that millions can access the care they need.
Your new role
In this role you will be at the intersection of science strategy and regulation ensuring Novo Nordisks portfolio maintains and expands its market presence through compliant and timely regulatory submissions. You will play a key part in translating our pipeline ambitions into approved treatments that reach patients worldwide.
Your key responsibilities will include:
- Preparing compiling and submitting regulatory applications and lifecycle management activities to health authorities across relevant markets
- Providing regulatory strategic input to cross-functional project teams to support product development and commercialisation timelines
- Monitoring and interpreting evolving regulatory requirements guidelines and legislation to ensure ongoing compliance
- Building and maintaining strong relationships with health authorities acting as a key point of contact during regulatory procedures
- Contributing to the development of labelling product information and promotional material review from a regulatory perspective
- Supporting due diligence activities and regulatory assessments for business development opportunities
- Collaborating closely with colleagues in medical affairs commercial strategy and quality to align regulatory activities with broader portfolio goals
Your new department
The Regulatory Affairs team plays a critical role in securing and maintaining market authorisations that enable our products to reach patients. You will join a collaborative team of regulatory professionals who work across therapy areas and geographies partnering with internal stakeholders and health authorities to navigate an increasingly complex regulatory environment. Your contribution will directly influence the speed and success with which our innovations become available to those who need them.
Your skills & qualifications
We are looking for a regulatory affairs professional who thrives in a dynamic science-driven environment and is motivated by the tangible impact of bringing treatments to patients. To succeed in this role you will bring:
- Bachelor degree in Life Sciences Pharmacy Medicine or a related field (MSc or PhD preferred)
- 3yrs experience in regulatory affairs within the pharmaceutical industry including hands-on involvement in regulatory submissions and lifecycle management
- Strong knowledge of regulatory frameworks and guidelines and the ability to interpret and apply evolving requirements
- Excellent communication and stakeholder management skills with the ability to convey complex regulatory information clearly to cross-functional teams
- A structured and detail-oriented approach combined with the ability to manage multiple projects and priorities simultaneously
- Fluency in English both written and spoken
- Thai citizen or permanent resident mandatory
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 youre not just starting a job youre 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.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. First nations people encouraged to apply.
At Novo Nordisk were not chasing quick fixes were creating lasting change for long-term health. For over 100 years weve 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 whats possible in healthcare. We embrace diverse perspectives seek out bold ideas and build partnerships rooted in shared purpose. Together were 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.
Required Experience:
Unclear Seniority
About Company
You will be part of the Gulf Cluster sales team based in Qatar. You will report to the Country Sales Manager. The local team consists of approx 10 employees, and has highly-engaged and experienced members that are looking for a new teammember.