Øvrige i Måløv

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Måløv

Are you passionate about setting direction and ensuring timely delivery of development products to our patients in clinical trials? Are you motivated by developing both processes and people and continuously improving engagement and performance? Do you possess management experience, and would you like to be part of building a new organisation in Parenteral Protein Formulation QA (PPF QA) as we are expanding? If so, we have an exciting opportunity for utilising both professional and people skills.

The Position

You will lead a team of 10-15 employees and refer to the Director in PPF QA. You will be part of a department consisting of three teams where you will head up “EarlyPhase and CMO” where the main tasks in the team are supporting our aseptic pilot plant, releasing batches for early phase clinical trials internally produced as well as from external CMO collaborations.

To be able to meet the new Annex 1 requirements for aseptic production there are different projects coming within the coming years to comply with the regulations. The major priority will be implementation of an isolator.

As the department just recently has gone through an organisational change, you will also have impact on establishing a new management group having a significant impact on the future strategic goals and directions within the department.

Your responsibilities include:

  • Being able to maintain an overview, follow up on performances and set directions for everyone in the team.

  • Ensuring the team solves the tasks timely under your guidance to work smarter and more efficiently.

  • Building and maintaining a close collaboration with the stakeholders and ensure common alignment.

  • Coordinating and exchanging experiences across teams and departments.

  • Increasing focus and utilisation of LEAN and new technology such as digitalisation and automation to improve both performance and the working environment across the department.


Qualifications

To succeed in this position, you:

  • Degree in pharmacy, engineering or equivalent background.

  • At least 2 years of relevant experience as a people manager.

  • Experience related to quality assurance and/or pharmaceutical production/GMP.

  • Experience working with CMOs is a plus.

  • Good communication skills both in Danish and English


In a personal way you are determined, decisive and have the will to take the lead both professionally and in collaboration with other professional groups - just as you dare to take the lead and pave the way in both team and department. Your natural sense of the right level of detail helps employees deliver what is needed.

You are proactively striving for higher levels of performance, not being afraid of being challenged by peers and employees.

You are well organized and create strong results by engaging your employees in taking pride in delivering on their objectives.

About the Department

The department is a part of CMC Development QA and located primarily in Måløv and Bagsværd with assignments in other production sites in the greater Copenhagen area as well. We also work with CMO´s worldwide. Currently, we are around 20 highly qualified employees with even more colleagues to join us soon. We are responsible for assuring the quality and compliance of our aseptic filling line in CMC, approve development documents, releasing all parenteral development batches for our clinical trials as well as supporting the business by improving and simplifying processes.

Working at Novo Nordisk

We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.

Contact

For further information, please contact Marianne Mørch Hansen +45 3079 8154.

Deadline

Apply before November 13, 2022.

You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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 8.7.2022, 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.
  • Øvrige
  • Måløv

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