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stillingsbetegnelse:
Regulatory Affairs Graduate: start changing your career!

jobbeskrivelse:

Looking for a life-changing career within R&D regulatory affairs? Use your master’s degree and join the 2-year Regulatory Affairs graduate programme. It will give you comprehensive knowledge of our regulatory work and of the drug development process, enabling you to find the niche where your competencies and interests coincide. This is a great opportunity for future regulatory leaders to gain international experience in a world-leading company where you can make a real difference to the millions of people who rely on our products.

 

About the Regulatory Affairs graduate programme 
In Novo Nordisk, Regulatory Affairs secure the approval of new multi-billion dollar products and drug indications, making it possible for the company to bring innovative products to patients. We stand at the centre of project planning and execution from the earliest stages of drug development all the way through life cycle management. The Regulatory Affairs graduate programme has been designed to develop top talents into becoming future leaders within this area.

 

During the programme you will work with senior managers and build an international network of world-class colleagues, establishing yourself as one of tomorrow’s key people in Regulatory Affairs at Novo Nordisk.

 

We’ve designed the Regulatory Affairs graduate programme so that, following its successful completion, you will be equipped with the necessary skills and experience to become an integral part of our company – typically with a permanent position in Denmark or elsewhere in our global organisation.

 

The position

During the 2-year programme you will undertake three rotations of 8-months duration. Two rotations will take place in our corporate headquarters in Denmark and one rotation will be in one of our global affiliates. Examples of recent international rotations include the US, China, Japan, Canada and Brazil.

 

The rotations are shaped to suit your development needs, while meeting our business requirements and to ensure you build the required competences needed to become one of “tomorrow’s key people” in Novo Nordisk. Below is an example of how the rotations could be shaped:

 

• Rotation 1
  Placed in a department in corporate headquarters with strong connections to Regulatory Affairs, you will be introduced to the regulatory trade and gain hands-on experience. Regulatory Affairs are closely integrated in the drug development and drug maintenance processes of Novo Nordisk. Hence, this rotation will give you the capacity to understand the business from the viewpoints of our partners, such as R&D and Product Supply.
   
• Rotation 2
  Working in one of our global affiliates or regional offices, you will gain insight into regulatory affairs work from a local perspective. You will work to ensure the timely submission of applications and subsequent approvals. Local regulations and different cultures make this a very interesting challenge, calling for great project management skills and deep insight into rules and regulations, and for negotiation and collaboration skills as you will liaise with different stakeholders in and outside of Novo Nordisk. This unique international perspective should prove invaluable as new markets continue to evolve for Novo Nordisk.
   
• Rotation 3
  During this placement back at our corporate headquarters, you will now be able to perform strongly in the role of a regulatory professional. You will manage important and complex projects as you help us realise our vision of achieving and sustaining best in class approvals.
   

Working at Novo Nordisk

As a world leader in diabetes care, working at Novo Nordisk allows you the opportunity to make a significant difference to patients and society, while also providing you with the ability to deliver exciting results from a business perspective in a global pharmaceutical company.

 

Joining Novo Nordisk should appeal to you not just because we respect and value our employees, but also because of what we do to change the lives of millions of people around the world. To work here you need to be highly ambitious, yet have a team player mind-set and enjoy working in a global and culturally diverse organisation.

 

Qualifications

To apply for the Regulatory Affairs graduate programme, you must have:

• A PhD or a master’s degree from 2018 or 2019 in a natural science, for example within pharmacy, chemical engineering, biology, biotechnology or a related field
  Please note: if you are graduating outside this timeframe then check out these opportunities: student jobs, internships and permanent entry level jobs
• A minimum of 6 months’ international experience from working, studying or voluntary work
• Relevant work experience or extracurricular activities obtained next to your studies
• No more than 1 years of work experience after finishing your master’s
• Above average academic achievements
• Strong analytical skills
• Excellent communication skills
• High drive and ambitious goals
• Eagerness to learn and willingness to challenge status quo
• An international mind-set and be globally mobile
• Team-player skills
• Professional fluency in English

 

If you meet all the criteria then apply now and no later than 8 January 2019 (GMT+1) by submitting your motivational letter and CV (in English) plus a copy of your master’s certificate or latest grade transcript.

In addition, you must provide a 1-minute video of yourself explaining why you are the ideal candidate for the Regulatory Affairs graduate programme.

 

Contact

See all our other graduate programmes, read current graduates’ blogs and learn more about the application process at novonordisk.com/graduate. For further information, please contact Karina Kokholm at knko (at) novonordisk.com or Elisabeth Buhl Thubron at ETHU (at) novonordisk.com.

 

Important: Prepare this before you apply
Before you click the “Apply now” button please ensure you have prepared a motivational cover letter, your CV and latest transcript.
To supplement the written information you will be asked to record a 1 minute video, where you are asked to answer: “Why am I the perfect candidate for this graduate programme?” Your video answer will be recorded as a part of the application process. Note that you will be able to record you answer several times before submitting. Tip! Meet candidates and Programme Managers in this video and hear their experiences with the application video.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2423

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: Novo Nordisk A/S

source: DK-STAR