ISO IDMP consultant - Regulatory Information Specialist

NNIT A/S

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Are you a specialist within the ISO standards for Identification of Medicinal Products (ISO IDMP)? Or do you have a solid background in Regulatory Affairs and Regulatory Information such as xEVMPD data and would like to become a specialist in ISO IDMP? Then you would be the ideal candidate to join NNIT’s cutting-edge ISO IDMP group, which is looking to recruit a new consultant.



Your responsibilities as ISO IDMP consultant

You will join NNIT’s recognized and successful ISO IDMP group, which consists of skilled and ambitious specialists that have a deep understanding of the ISO IDMP standards and the ability to bridge this knowledge with IT. Working closely with colleagues and clients, we use our experience to advise and assist life sciences companies in a vast array of projects spanning from vendor selection, data analysis, process optimization and adaptation to the forthcoming changes.



A central part of the job is to join NNIT’s advisory projects for international clients, with a high degree of responsibility for project execution and communication. You would also be expected to play an important role in continuously developing the group’s competences and knowledge. The job will also include close collaboration with a multitude of stakeholders where your knowledge from the pharmaceutical industry will strengthen our company’s strategic aspirations in life sciences.





You will join our ISO IDMP group

You will become part of our ISO IDMP group which is part of the Life Science Advisory department.



In NNIT we ensure that your personal career aspirations are continuously evaluated and that you develop in your respective position. We will ensure that your qualifications match the high requirements faced by our clients.



Our clients expect that we are at the forefront of upcoming trends and legislative changes such as ISO IDMP, and that we are able to transform our knowledge into concrete advice and solutions. Your career will therefore include continuous education supporting our department and your personal aspirations. You would be expected to participate in conferences, teaching and other knowledge exchange with colleagues and clients.



The department is part of the Solutions division responsible for advising our customers on business and technology as well as designing and implementing IT solutions and applications.





Your qualifications and experience

You hold an academic degree in e.g. IT, business or life sciences. You have at least 3 years of experience from the pharmaceutical industry or consultancies, or 5-8 years of experience, if applying for a principal consultant position. You have a good understanding of core disciplines within IT such as information management, requirements specification, project delivery etc. and you are able to bridge your professional experience from the pharmaceutical industry, preferably Regulatory Affairs or Pharmacovigilance, directly with IT.



Fluent oral and written English is a must. German is an advantage.