QA Professional, Qualified Persons Delegate

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Måløv

Are you a truly skilled and proficient person? Do you master GMP, and Quality related to packaging and supplying products for clinical trials - or are you eager to master this? Do you demonstrate a high level of energy, motivation, and diplomacy. Then I may have just the right job for you in CMC Clinical Supplies QA.

About the area

Novo Nordisk is going into new therapeutic areas. The portfolio is growing and diversifying as ever before. Numbers of patients, countries and sites participating in our clinical trials are increasing. Thus, we are seeking a new colleague in CMC Clinical Supplies QA to be part of this fantastic effort. We are part of the Novo Nordisk Quality organisation where we enforce compliance on behalf of authorities and patients, support the business and at the same time strive towards making daily work for ourselves and our stakeholders less complex – always having the Novo Nordisk Quality Mission in sight: Highest Quality for Patients.

The job

Your will work as a QA for the Clinical Supplies area.

You will act as a QP delegate to certify and release the final packaged product.

We work at the borderline of GMP and GCP and you must be able to consider both aspects of regulations and reach out and obtain knowledge at this borderline. Regulations and ways of setting up and conducting clinical trials are evolving rapidly these years, so you must be able to adapt to and enjoy these changing times within your daily work.

Depending on you level of experience and ability to act across, you will contribute to improvement projects both internally with our stakeholders, but also across the NN Quality organisation where we continuously strive towards taking our Q processes to the next level.

Qualifications

We are looking for candidates with

  • Master’s degree in pharmaceuticals, medicine, veterinary science, pharmaceutical chemistry and technology, chemistry or biology.
  • Experience with GMP related to the pharmaceutical industry, preferable manufacturing for clinical trials.

You will work with multiple stakeholders across the organization. You have great stakeholder management skills and the ability to handle conflicting interests and evaluate issues from all perspectives. You must be able to take and communicate decisions in an effective way.

Good analytical skills and an ability to evaluate the full picture is a requirement, since complex cases will have to be handled on a daily basis. The ability to work and deliver results independently and at the same time be a team player and make your colleagues shine is necessary.

Working at Novo Nordisk

Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.

Contact

For clarifications or questions, please contact Birthe Rottwitt at +45 3075 0158.

Deadline

December 1st. We will look at applications and perform interviews continuously - and hire if the perfect match is found prior to this deadline. It might be you. We are eager to welcome our new colleague.

To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

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Information og data

Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 28.10.2022, 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.
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