Experienced Validation responsible in R&D IT - Safety & Regulatory Solutions

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  • Information Technology & Telecom
  • Bagsværd

At Novo Nordisk, we have a passion for improving patients’ lives all over the world. Will you help us bringing that passion to life? Would you like to further develop your expertise within validation, QC and test automation? Would you also like to be part of large-scale agile projects? If you do, please apply and become the newest member of the Research & Development IT organization.

About the department

You will be part of the Safety & Regulatory Solutions Department, belonging to Research & Development IT, located in Søborg and Bagsværd - Denmark. We are a dedicated team of 23 people, responsible for the implementation & development, support & maintenance and operation of Global R&D IT applications. We are all working together as part of an agile, inspiring and ambitious team.

Our aim is to increase the value generation to our business stakeholders through the implementation and development of Digital Solutions. Those solutions span across many areas and technologies, but the central objective is to explore new ways of creating value from our vast data repositories and to automate and improve our manual work processes.

Currently the department is fully dedicated to drive the digital transformation in both Safety and Regulatory Affairs.

The job

This is a job for a person who is excited to work with technologies and doing validation, testing and QC for agile IT projects.

Key tasks include participation in large scale IT projects in R&D as the validation expert and executer of validation and QC activities. You take responsibility for all validation activities for the project(s) e.g. planning, documentation, coordination and reporting and you are quality-minded with good ability to execute within deadlines. You also help develop and optimize our approach to validation and QC work, ensuring we test and validate the right things on the right level. You are comfortable making trade-offs and participate in risk analyses, allowing a risk-based approach to testing. You drive and execute the project’s test automation and take the lead on increasing our level of test automation.

Qualifications

You have completed a Master’s degree within Computer Science, Engineering, Software Development or other related field. Alternatively, to a Master’s degree, you have proven and extensive experience within IT Validation in the pharma industry. You are experienced in working with large scale projects and validation, preferably working in an agile manner. Having experience from validation in a GXP environment, is a clear advantage. Experience with test automation and the tooling around it will be a clear advantage.

Contact

For further information, please contact Sebastiaan Van den Wijngaert at +45 30775921.

Deadline

Submit your applications no later than 25-AUG-2020 and note that relevant candidates may be invited for interview on an ongoing basis before the deadline.

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.


Information og data

Denne ledige stilling har jobtypen "Teknisk sundhedsmedarbejder", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Bagsværd.

Jobbet er oprettet på vores service den 30.6.2020, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Teknisk sundhedsmedarbejder
  • Bagsværd
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