Associate Regulatory Professional
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Søborg
Would you like to work on regulatory submissions across Novo Nordisk portfolio in a global environment where we bring innovative treatment to patients worldwide? Does driving, coordinating, and working with colleagues from many different professional backgrounds and cultures inspire you? 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; these at various stages and with overlapping and often challenging timelines where excellent navigation skills are essential. You will work in a fast-paced environment and the role requires the ability to work effectively with people across the organisation, requiring a high level of 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 stakeholder interactions. Qualifications To succeed in this role, we expect you to have: A master’s 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 On a personal note, you possess excellent communication abilities and a proactive, solution-oriented mindset. You are a flexible and change-ready 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 have 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 which is one of the two head quarter based regulatory functions. We are responsible for the additional regulatory documents process obtaining national documentation, in compliance with health authority regulations, to worldwide submissions, and have the privilege of working across Novo Nordisk product portfolio. We are 13 dedicated and highly engaged employees in the department with diverse background and experience. We have a broad and 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. The atmosphere is informal, and a good sense of humour is always 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 29 October 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.
Information og data
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 10.10.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Søborg
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