Scientist for Cleaning validation and production support

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Are you curious about Cleaning Processes during GMP production in a multi-product facility? Are you driven by optimizing cleaning processes, positively affecting equipment down time and saving resources? And do you thrive in a dynamic environment which combines both daily operations and long-term improvements? Then you might join our team as cleaning responsible, and together ensure our daily operations and future productions.

The position
As Cleaning Responsible you will join a team of skilled and motivated colleagues responsible for cleaning support of a broad variety of production equipment and processes in our Cultivation Pilot Plants, focusing on optimisation and stable performance.

You will use your scientific/technical knowledge and process understanding to contribute to the cleaning strategies for our multi-product facilities, support production in daily operation and with deviation handling, optimisation of Cleaning in Place (CIP) processes, and cleaning validation of new and existing equipment, all following the standards of the pharmaceutical industry (GMP).
Additionally, you will be taking on projects for implementation of new equipment, this includes design, support, and report of the implementation of cleaning validation plans and ensuring continued cleaning verification.

There will be opportunities for you to get involved and take part in cross-organisational tasks, projects, and problem solving, where you will be able to influence processes and professional standards across a larger organisational area.
The position gives you a great opportunity to play a key role in optimisation, problem solving and ensuring that the solutions are in line with industry standards. You can also look forward to joining a social and informal team that thrives on exciting professional challenges and works independently with a high level of commitment.

Qualifications
You hold a degree, MSc or PhD within Science, Engineering or Pharmacy.
Preferably, you have:
• experience in the pharmaceutical or biotech industry and have solid experience with cleaning (Cleaning in place, cleaning validation).
• a systematic approach to daily tasks, problem solving, and cleaning projects
• theoretical and practical experience with conducting cleaning activities in connection with GMP production.
• excellent collaboration and communication skills
• a proactive and solution-oriented mindset

• understands and speak Danish
As a person you are able to work independently, you set directions and you are able to handle a complex and sometimes hectic workday. You are flexible and have the courage and drive to engage in new assignments and stick to them until the job is finished.

About the department
The position is in the department Cultivation Pilot Plants and part of Chemistry Manufacturing and Control (CMC) API Pilots. CMC API Pilots is a part of the R&D organisation, that manufactures and controls new drug substance candidates for the development portfolio at Novo Nordisk.

Cultivation Pilot Plants is a department that cultivates and purifies proteins and peptides, for use in clinical and non-clinical trials. The department consists of two separate production facilities with four production lines in total.
In the department we work with various technologies and equipment depending on whether the cultivation is based on yeast, E. coli or mammalian cells, and on how the recovery process is designed (i.e. centrifugation, filtration, chromatography etc.).
While we need to ensure efficient production capacity, we also have an eye on the future, making sure that we utilise the opportunities technology provides, i.e. automation and robot technology.

The department is located in Bagsværd, Denmark.

Working at Novo Nordisk
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.

Contact
For further information about the position, please contact Tine Kranker at +45 3075 5156

Deadline

14th January 2023.

We will be conducting interviews on an ongoing basis, so we encourage you to apply as soon as possible.
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 Bagsværd.

Jobbet er oprettet på vores service den 27.9.2022, 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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