GCM CMO supporter

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Bagsværd

Are you passionate about working with contract manufacturing and thriving in a dynamic and international environment with many stakeholders? Are you up for involvement in a variety of products and GMP environment? If you are ready for further learning and development opportunities then you might be the new Supporter we are looking for to join our department, Global Contract Manufacturing Support (GCM-S)

We offer you an exciting job in an international environment with the possibility to play an important role in Novo Nordisk Contract Manufacturing Organisation together with our specialists who work with projects at our CMOs and with a broad network across Novo Nordisk.
You will join an experienced and talented team where we have an informal and direct tone and where we value each other’s differences.

The department

Our unit, called Global Contract Manufacturing, is a part of Novo Nordisk’s Product Supply organisation and responsible for Novo Nordisk contract manufacturing of API, intermediates, side chains, semi-finished and finished drug products to global markets.
Our main office is in Bagsværd, Denmark.

The primary role as Global Contract Manufacturing Support is to implement new projects at existing and new CMOs. The projects are managed by GCM in collaboration with our development organisations.
Furthermore, our department supports the production at our CMOs in operation with certain tasks that require expertise and knowledge of the production processes. Our CMOs are located all over the world.

In GCM Support, you will join a department of 17 highly dedicated, experienced and talented colleagues. We are dedicated to ensure that contract manufacturing strengthens Novo Nordisk supply chain by sourcing products into Novo Nordisk according to the demand from our production sites and customers world-wide.

The position

As Supporter in GCM, your overall objective is to comprehensively support the entire department with project tasks, handling of deviations, change control requests, LIMS set-up and other important tasks, to ensure projects can be executed timely. Furthermore:

  • You will be responsible for sampling setup, data analysis and coordination and data maintenance using for instance the LIMS system.
  • Responsible for coordinating and establish technical documents for CMO or for the authorities incl. review of master batch records for process validation batches.

You will be an independent and self-driven contributor towards the company’s work objectives. You will have a wide range of stakeholders, both internally and externally and you will cooperate closely with our Specialist, Quality and Logistics departments.

Qualifications

You hold an academic degree within a relevant discipline, e.g. Engineering, Pharmacy or have relevant experience, typically obtained from a pharmaceutical production. We also encourage recently graduated candidates to apply and we will ensure the necessary training. Furthermore:

  • Knowledge and/or some experience within GMP environment.
  • Interested in and/or some experience within medical/pharma, LIMS system, deviations and change control handling.
  • Good communication skills and a structured approach to the tasks at hand, in order to gain commitment from both internal and external stakeholders.
  • You enjoy working independently and proactively in a dynamic environment, with many tasks to coordinate and execute on, changing priorities and strict deadlines.
  • Fluent in written and spoken English.

You have a positive and open mind-set and you are good at building relationship and communicating across cultures.

Our CMOs are located around the world; hence minor travel activity might be expected

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 Thomas Lindblad at +45 3075 5179

Deadline

16th January 2023

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 Bagsværd.

Jobbet er oprettet på vores service den 13.12.2022, 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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