Associate Regulatory Professional

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Søborg

Are you curious about working with regulatory submissions across Novo Nordisk product portfolio? Are you inspired by driving, coordinating, and collaborating globally with colleagues from different backgrounds and cultures? Then we offer you this exciting opportunity in Regulatory Affiliate Support. Apply today and join us for a life-changing career! The position As an Associate Regulatory Professional, you will be the centre of planning, coordination, and execution of national registration file documentation such as export certificates and statements as well as product samples critical for submissions to health authorities worldwide. To obtain fast submissions and regulatory approvals, you are expected to assess regulatory requirements and local regulations and provide solutions accordingly. You will act as central point of contact for affiliates and continuously be involved in several submissions across Novo Nordisk product portfolio. These submissions will be at various stages, often with overlapping challenging timelines. You will work in a fast-paced environment and the role requires the ability to work effectively with people across the organisation, calling for high cultural awareness and the necessary skills to take the lead, encourage and influence. You are expected to bring forward regulatory insight, be proactive and take actively part in discussions and interactions. Qualifications To succeed in this role, we expect you to have:
  • University degree in a relevant field such as life or health science, pharmacy, or business, and preferably some experience from the pharmaceutical industry
  • Excellent communication skills and are comfortable and competent to communicate in both verbal and written English
  • Business and process orientation
  • Flair for IT systems
    • As a person, you bring a can-do spirit and a healthy sense of humour to work. You are a flexible and change-oriented person who likes to experiment and sees opportunities rather than limitations in challenging situations. It is imperative that you are well organized, can handle tight deadlines, and manage multiple assignments without losing track. You possess strong analytical skills and problem-solving capabilities and address your responsibilities with decisiveness and a positive mind-set. About the department Regulatory Affiliate Support is located within the area of Regulatory Affairs CMC & Devices, and we are responsible for the additional regulatory documents process supporting submissions worldwide and across Novo Nordisk product portfolio. We are 13 dedicated and highly engaged employees in the department with diverse background and experience. We have a strong collaboration with our stakeholders across the organisation both within headquarters as well as affiliates. In Regulatory Affiliate Support, we seek continuously to improve our processes to support fast submissions and approvals, and to ensure compliance with the global regulatory landscape which is constantly changing. We have an informal environment where a good sense of humour is welcome. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Tina Lindquist at +45 3075 9652. Deadline 02 July 2023. Applications will be reviewed continuously, and we will conduct interviews on an ongoing basis, so please submit your application as soon as possible. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.


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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Søborg.

    Jobbet er oprettet på vores service den 15.6.2023, men kan have været deaktiveret og genaktiveret igen.

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    • Søborg
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