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reference: 4951821

documentId: 4951821

connectionPointId: 7

lastModificationDate: 1551275235380

stillingsbetegnelse:
Regulatory Professional in Regulatory Operations (temporary)

jobbeskrivelse:

To support our world-wide regulatory submissions, we are seeking two Regulatory Professionals to join the Regulatory Affiliate Support department in temporary positions for a period of two years.

 

About the department

Regulatory Affiliate Support is part of the Submission Management area in Regulatory Operations, located in Søborg, Denmark. We work closely with stakeholders across the organisation both within headquarters in Denmark and India as well as affiliates worldwide. We are a team of 8 highly motivated and engaged employees who are responsible for the additional regulatory documents process supporting global submissions.

 

The position

Your main responsibility as a Regulatory Professional is to be central point of contact for affiliates and provide them with additional registration file documentation such as export certificates and statements as well as product samples for submissions to health authorities worldwide. One of your focus areas is to support global manufacturing site transfers ensuring timely submissions of these. 

You will be interacting with many stakeholders in the company and with health authorities in order to provide responses and documentation to support the submissions. In addition you will be planning, coordinating incoming requests as well as assessing regulatory requirements and finding solutions to these.

 

Qualifications

You hold a Master’s degree in e.g. Business/Science/Pharmacy/Medicine combined with a strong business and process orientation. Preferably you have experience from the pharmaceutical industry. 

We expect that you are able to drive activities and tasks independently and systematically and that you enjoy working in a dynamic environment. You are able to stay on target, work with tight deadlines and manage multiple assignments at the same time without losing track. You have very good analytical skills and problem solving abilities and address your responsibilities with decisiveness and a positive mind set. 

You have advanced communication skills as well as experience with presenting in large forums as stakeholder management and communication are essential for succeeding in the job. Furthermore, we expect that you possess strong cross-cultural skills and are used to working with international business partners. Finally, full professional proficiency in oral and written English is a must.

 

Working at Novo Nordisk

In Novo Nordisk, it is your skills, your commitment and your ambitions which help us to improve many people’s lives. In return we offer you the opportunity to work with talented colleagues and we offer you a wide range of opportunities for professional and personal development.

 

Contact

For further information, please contact Tina Lindquist at +45 3075 9652.

 

Deadline

12 March 2019.

 

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/C3213

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