Writer with a flair for simplicity
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Søborg
- Quality
- Søborg
Are you ready to make an impact on the processes owned in Medical Affairs, Regulatory and Safety (MARS) by re-writing Standard Operating Procedures (SOPs) to become simple, user-friendly, and clear? Then you might be the person we are looking for a temporary 12 month maternity cover in MARS Quality
The position
You will play a key role in simplifying the SOPs in MARS by performing re-writes to cut complexity and enable simplification of processes. To be successful in SOP simplification you will need to collaborate across the MARS areas with different stakeholders across the world, where your writing and communication skills will help you succeed.
The MARS processes are described in SOPs, and the organisation is continuously striving to simplify their processes. You will lead project activities related to SOP writing, facilitate process mapping, and coordinate successful finalisation of SOPs. Specifically you will be working on projects with aim to transform our ways of working. Therefore it is also important that you have an agile mindset and flair for organisational change management.
This is a unique opportunity to develop knowledge of many processes within Regulatory Affairs and Global Safety, and you will also develop skills within Quality, learning about external requirements for the pharmaceutical industry and how to implement them in SOPs.
Qualifications
You have an MSc degree and experience in clearly written documentation, project management, and/or communication. The role requires the ability to communicate complex information in a simple way. You have a strong sense of structure, and are able balance business needs, tasks/resources, deadlines, and find the right level of detail.
- Ideally you have experience in the following areas: Developing training materials or user guidance
- Learning new information and writing about it
- Using IT systems in a smart way, especially Word or document management systems
- Facilitating work in small groups, especially document review
- Collaborating with people from diverse professional backgrounds
As person you are team-oriented with a high degree of flexibility and change readiness. You are highly motivated, self-driven, and visionary within your field of expertise.
About the department
You will be joining the MARS Quality department consisting of 25 highly engaged employees, located in Bagsværd, Søborg and Bangalore with different professional backgrounds. You will be a part of the MARS QA team consisting of 10 employees who have expertise within quality processes like SOPs, Deviations, Change Control, Audits and Process Reviews. We collaborate with a wide range of stakeholders spanning across the MARS organisation, NN Quality and affiliates.
Working at Novo Nordisk
Novo Nordisk is one of the world’s most successful pharmaceutical companies and with a strong growth potential. At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information please contact MARS Quality Manager Karina Kokholm at +45 3079 8101.
Deadline
30 November 2020.
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 chronic 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.
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 17.11.2020, 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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