QA Validation Specialist

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Hillerød

  • Quality
  • Hillerød

Do you have a strong background within Process Validation and a talent for driving simplification of processes? Do you also have practical experience from validation of manufacturing processes? And do you thrive in sharing your professional insights and have the communication skills to function as a source of knowledge for a host of dedicated colleagues across the organisation? Then you might be the person we are looking for in Device Manufacturing Development QA (DMD QA) in Hillerød.

About the department
In DMD QA we are 26 highly qualified employees divided into 3 teams. We are located in building 24K at Site Hillerød and we are responsible for assuring quality and compliance of all processes in Device Manufacturing Development (DMD). Both internally in DMD and in the rest of Novo Nordisk we have many key stakeholders due to the nature of the processes in Device Manufacturing Development. We are constantly improving our competences and our way of working by focusing on simplicity, agility and collaboration for us to be able to deliver the best possible support to the business.

The position
As our QA validation specialist your main task will be, together with your QA colleagues and Line of Business, to ensure effective implementation of the new “Science and Risk based validation” concept. You will get the responsibility as D&S Validation Process Group QA and as such it will be expected that you act as a role model when giving support and advice on process validation.

You will also be responsible for delivering QA validation support to FP Manufacturing Intelligence - a relatively new established department in DMD supporting all FP (finished products) sites in Novo Nordisk with Machine Learning solutions and other associated technologies.

In other words, you will be quite visible in the QA organisation, being the specialist that colleagues and management will rely on to support our process validation approach. You will have a broad stakeholder landscape to navigate in, - both across and within the quality organisation and also within DMD and our finished product production sites worldwide.

Qualifications
You have a Master degree within pharmacy, engineering or similar and preferable 5-10 years of experience from the pharmaceutical industry within process validation.

You are ready to take on responsibility, and you convey your knowledge and experience with a steady hand. We expect you to build trustful relations across the organisation and to competently enjoy being the expert your colleagues can count on for advice and sparring. You use your excellent cooperation skills when you manage your stakeholders both in- and externally to ensure reaching solutions that will meet both requirements and stakeholder interests. You are seen as well-organised, independent and have a flexible but firm approach.

You are attracted by the opportunity to use your quality skills in a highly complex and ever-changing working environment. As we work in a global business environment, we expect you to be proficient in English, in speech as well as in writing.

Working at Novo Nordisk

At Novo Nordisk, you will join a patient-centred culture of talented professionals. We respect individuality and empower you to make the most of your potential. At Novo Nordisk we use our skills, dedication and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.

Contact
For further information, please contact Inger Sørensen at +45 3075 4648.

Deadline
08 March 2020.

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 "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Hillerød.

Jobbet er oprettet på vores service den 5.3.2020, 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.
  • Øvrige
  • Hillerød
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