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IT Validation and Compliance Specialist I
3 days ago
Department – Submissions, Labelling & Translations solutions - Digital Data (DD) & IT Development GBS
Are you experienced in IT validation and compliance within the pharmaceutical industry? Are you looking for a new challenge in a global healthcare company? We are seeking an IT Validation and Compliance Specialist I to join our DD&IT Development GBS Regulatory Solutions at Novo Nordisk. If you have a strong background in computer system validation and a passion for ensuring regulatory compliance, then read on and apply today for a life-changing career.
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About the department
In DD&IT Development GBS – Submissions, Labelling & Translations Solutions, a part of DD&IT GBS, a portfolio of GxP & business critical applications is being managed and supported. These applications are among the most critical IT systems in Novo Nordisk supporting essential processes and being used 24x7 by thousands of users worldwide. We work closely with line of Business, System managers, Quality Check (QC)/Quality Assurance (QA) and subject matter experts across the Novo Nordisk IT organization in Denmark and India. We work in Submissions and Labelling (SuLa) ART.
The position
As an IT Validation and Compliance Specialist I, at Novo Nordisk, you will have the following responsibilities:
Qualifications
To be successful in this role, you should have the following qualifications:
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