id: NTAyMTI5NSA3

reference: 5021295

documentId: 5021295

connectionPointId: 7

lastModificationDate: 1563798672340

stillingsbetegnelse: Regulatory Affairs - Senior Consultants

jobbeskrivelse:

Use your pharmaceutical experience to transform Regulatory Affairs

NNIT is looking for several senior consultants with a deep pharmaceutical expertise who wish to make a mark on some of the most exciting IT projects within the Life Sciences industry.

The NNIT Regulatory Affairs Advisory team is on the forefront of advising global pharmaceutical clients on the latest changes within Regulatory Affairs and the IT impact to the industry. Are you our new colleague?

Your responsibilities as a Senior Regulatory Affairs Consultant  

You will join an exciting, international advisory department with highly skilled colleagues that have a deep understanding of the pharmaceutical industry and the ability to bridge this knowledge with IT.  

Working closely with international clients, you will use your experience from Regulatory Affairs to:

• Advise and assist companies in a vast array of projects, spanning from RA process optimization to new regulatory changes.
• Advice on vendor selections for new IT solutions within the area of electronic document management systems (EDMS), eCTD, labelling and regulatory information management systems (RIMS).
• Give presentations and speaker sessions at conferences and write articles about Regulatory Affairs topics.  

A key part of the job is business development activities related to new offerings that will support our continued growth within the areas of Regulatory Affairs and Pharmacovigilance. The job will include close collaboration with a multitude of stakeholders within NNIT where your specialist knowledge will strengthen our companies' strategic aspirations in Regulatory Affairs.

You will be part of NNIT’s Life Sciences Advisory

NNIT’s Life Sciences Advisory is an ambitious department of a key importance to NNIT’s strategy. We appreciate openness, honesty and a winning attitude. We expect you to have these personal skills and expect that you are able to quickly integrate with the other team members.  

Our customers expect us to know about upcoming trends and regulatory changes, as well as, being at the forefront, in terms of technical solutions. Your career will include continuous training and competence development to support our department and your personal ambitions. 

NNIT was recently nominated as the most attractive workplace within the IT consulting area in Denmark.   

Your qualifications and experiences  

You hold an MSc degree in Life sciences or IT with 3-5 years of experience from the pharmaceutical industry (preferably Regulatory Affairs).

• You have a sound understanding of IT, and you manage to bridge your professional experience from the pharmaceutical industry with IT
• As a person you have a curious nature and interest in new technologies.
• It is an advantage if you have experience with business processes and regulatory requirements within Regulatory Affairs and that you have a good overall understanding of IT solutions within this area
• You may also have knowledge of Pharmacovigilance or Medical Devices processes and systems

You are used to advising and building trust on all levels, and you might have gained this experience from a past job within the consulting area. NNIT has offices in Copenhagen, Frankfurt and Basel, and we will expect you to live in the proximity of these pharma hubs. 

Fluency in oral and written English is a must. German or Danish is beneficial. Some travel must be expected.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2512

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: NNIT A/S

source: DK-STAR