Manager for Global Clinical Processes & IT in R&D Quality

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Søborg

  • Quality
  • Søborg

Do you wish to work in a highly professional, engaged and global environment where you can use your leadership experience, solid GCP knowledge, process optimisation skills? Where you can use your quality mind-set bringing clinical projects to registration and market? Then you may be the new Manager we are looking for!

About the department

The R&D Quality area is a part of Global Development, where we take responsibility for new products based on proteins and peptides from early development phases to product introduction. We are responsible for managing clinical drug development worldwide, securing that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society.

R&D Quality is divided into three departments. The open position is as Manager for the Global Clinical Processes & IT department. The department is responsible for clinical and non-clinical deviations, serious breach handling, IT quality support and QA, CAPA for devices, vendor assessments as well as providing Good Clinical Practice advice to the organisation.

The Position

As our new Manager, you will be responsible for managing your team of currently 8 employees. Your main objective is to drive continuous improvements to ensure we have competitive speed, flexibility and business quality whilst maintaining full compliance with external GxP regulatory requirements (incl. ISO for devices).

Your primary tasks will be to:

  • Head a team of 8 dedicated employees
  • Deliver continuous process optimisations that ensures compliant and efficient processes
  • Be QA responsible for deviations and specific IT systems used in Global Development
  • Build and nurture a team culture of mutual trust, cooperation and common drive
  • Coach, guide and develop your team members in a positive and inspiring way

You will be part of the R&D Quality management team which consists of the managers of the two other departments, the VP of Global Clinical Compliance and the CVP of the R&D Quality.

Qualifications

You have a degree in pharmacy, medicine, science or similar and a strong command of written and spoken English. You have at least five years’ experience in clinical research and drug development, as well as solid knowledge of GCP and other relevant regulations. Experience with clinical quality assurance, trial management, or monitoring as well as leadership experience is required.

You take a pragmatic approach to problem solving and have strong interpersonal skills. You are well organised and quality-conscious. You are a team player who adapts easily to a changing environment with tight deadlines. Additionally, you keep calm and result oriented under pressure and you have flair for planning, coordinating and reaching consensus with your stakeholders.

Working at Novo Nordisk

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, 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 Hanne Lang at +45 30791989 or Susanne Nørskov at +45 30 79 81 51.

Deadline

We will be screening and interviewing on an ongoing basis with a deadline of 20 October 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 "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Søborg.

Jobbet er oprettet på vores service den 11.10.2019, men kan have været deaktiveret og genaktiveret igen.

Rapportér
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Forsker
  • Søborg
Rapportér

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