IT Validation and Compliance responsible in DFP Site Hillerød

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Hillerød

  • Legal, Compliance & Audit
  • Hillerød

This is your opportunity to join Novo Nordisk, world leader in diabetes care, and become part of a dynamic and global environment. We are looking for a quality minded person who will ensure high quality in our portfolio of IT projects as well as in our daily business. Quality is a core element in our daily IT deliverables related to our critical IT Systems across Diabetes Finished Products (DFP) Site Hillerød.

About the department

You will be part of the Local IT Compliance and System Management unit consisting of 11 highly skilled System Managers, Analysts, Compliance and GMP Coordinators and Architects with daily collaboration with end-users, colleagues and stakeholders across the site as well as with vendors. We work in a unit with the aim to secure high quality and compliance of the Sites critical IT systems and infrastructure settings.

Our main focus is on IT governance, security, planning, management, minor projects and our license to operate. The department is characterised by strong collaboration and good team spirit, and functions as anchor point for IT-functions and projects across DFP Site Hillerød.

The position
Your assignment will be on one or more projects where you will join the IT and Compliance team. You will work closely together with Project Management and Local IT QA, to determine the right quality strategy and subsequently, ensure that project deliverables are of the right quality and in accordance with internal and external quality requirements. You will be a part of a team where you will be responsible for preparation and creation of validation protocols, performing validation tests, deviation and SOP handing and write final validation reports.

You will work in close collaboration with end users, local system managers, project managers, engineering partners and specialists in order to develop optimal solutions for the production.

Qualifications
You are dedicated with a quality mind-set. You have 2-3 years of experience within quality, preferably from IT companies, the pharmaceutical industry or the finance sector. You have a strong sense of responsibility for meeting objectives, are familiar with GMP requirements and you are considered as an enthusiastic and engaging team player with a positive attitude. You enjoy working in projects, where you have one or more full project life-cycle experiences. You are prepared to work with tight deadlines while maintaining a good sense of humour. You hold a relevant academic degree or have completed another relevant education. Good written and oral communication skills in Danish and English are a prerequisite.

Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Joan Frederiksen +45 3079 1128 or Mette Møller +45 3079 5133. Please note that applications will be reviewed on a continuous basis.

Deadline

11 August 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.


Information og data

Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".

Arbejdsstedet er beliggende i Hillerød.

Jobbet er oprettet på vores service den 10.7.2019, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Projektleder
  • Hillerød
  • Søndag den 11. august 2019

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