Regulatory Writer
Novo Nordisk
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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Regulatory WriterCategory: ManufacturingLocation:Søborg, Capital Region of Denmark, DKDo you wish to assist Novo Nordisk ensuring a robust and stable supply of its products across the globe?You can do this by being a part of our regulatory writing team, come join us!The positionThe regulatory documents behind submissions of new products, transfers of current products and changes made to our existing portfolio, are essential for us to meet our product supply demands at our own Novo Nordisk production sites globally, as well as contract manufacturing organisations around the world.At Novo Nordisk, we are experiencing an unprecedented demand for our products, and we aim to support this bold supply challenge with effective and courageous efforts to provide speedy, accurate and concise regulatory documentation in order to meet to this challenge.In this role, you will be responsible for:
QualificationsTo succeed in this role, we expect you to have:
On a personal note, you are meticulous, organized and have a structured and detail-oriented approach to everything you do. You take pride in delivering high quality documents and to do so you build and create a network to improve your knowledge and skills.About the departmentOur team sits within the Site Support and Improvement department, within IFP Manufacturing Development. Our purpose is to support the sites with our expertise process and product knowledge for marketed products and ensure that future manufacturing is possible by supporting product launches and transfers.
We are surrounded by Manufacturing development experts, who all also ensure that our products can get out to our patients as effectively as possible, regarding compliance, requirements from authorities and improvement and innovative opportunities.
We work across the departments, as one Manufacturing Development organisation.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, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.ContactFor further information, please call Senior Manager; Anneka Hastings at +4530798503Deadline16th July 2024
Please note that applications will be assessed on an ongoing basis and therefore the advert may close before the recruitment process is completed if we have proceeded with candidates to the screening or interview phase.
To apply, please submit your CV and a cover letter highlighting your experience and qualifications for this role. 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.
Søborg, Hovedstaden
Wed, 03 Jul 2024 01:08:02 GMT
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