Quality Assurance of tablet facilities

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Måløv

  • Quality
  • Måløv

Do you want to be part of the team assuring the quality of our new tablet production facilities? Novo Nordisk has built a new factory in Måløv which will be part of setting new standards for diabetes treatment going from project phase to operation. To succeed with this ambition, we need people with high level of team spirit, that have high engagement and that thrive in a constant changing environment.

About the department

In 2004 an ambitious and path-breaking journey began for us to become the first medical company delivering GLP-1-based tablets to the market. In 2020 we delivered Rybelsus® tablets to the first patients and going forward millions of patients with type-2 diabetes will have an oral alternative to injectable preparation. This is a result of competent, innovative and engaged employees’ efforts across the organization, who are proud to use their dedication to make totally new standards within the diabetes treatment. Join us at our journey – a possibility to make a personal and professional development.

Oral Finished Products QA is a department with approximately 25-30 skilled and motivated colleagues, who work with assuring quality and compliance of the facility, the equipment, product as well as the quality management system.

The job

In close cooperation with your colleagues in QA, you act as a QA for the facility, equipment and the quality management system. You contribute to finding solutions for ad hoc questions and challenges within compliance of cGMP facilities. The job is related to daily operation and qualification/validation of equipment and facilities for oral drug product manufacture. You will assure that the documentation for implementation and maintenance of equipment is compliant with internal and external requirements.

Furthermore, you will approve facility related documentation needed for the operation of the plant such as change requests, non-conformities, SOP’s, as well as trend reports for environmental monitoring and utilities.

Our continuing high level of audit and inspection readiness is on top of your agenda. This means you will be working with QA oversight where you are proactive together with your colleagues, to identify areas where our compliance can be strengthened. You have a risk based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct.

Qualifications

Ideally, you have a master in Pharmacy, Chemical Eng. or corresponding qualifications and at least some years of experience within the pharmaceutical industry. You have knowledge within some of the following areas: GMP, validation/qualification, analytical equipment for In Process Controls, equipment used in pharmaceutical production.

You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. Also, you are quite adaptable and challenge our way of doing things, so that we will get even better. You focus on results and quality – and contribute to the right level of compliance. Furthermore, you are proactive about being at shop floor and ensure continues improvements.

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 Rabab Bolø +45 3075 9628.

Deadline

26 July 2020. We will conduct interviews continually.

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 "Produktchef", og befinder sig i kategorien "Ledelse og personale".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 3.7.2020, 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.
  • Produktchef
  • Måløv
  • Søndag den 26. juli 2020

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