Development Scientist

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Bagsværd

Are you passionate about contributing your expertise in synthetic organic chemistry and scientific knowledge to support the life cycle management of our pharmaceutical products in a dynamic, cross-functional environment? Do you thrive in collaborating with diverse stakeholders, drive process optimisation and ensure the highest standards in technical documentation without the need for practical laboratory work? If so, join us as our new Development Scientist in Bagsværd! The position You will play a key role in the manufacturing of chemical moieties and/or the chemical modification of recombinant peptides and proteins. Supporting life cycle management activities at Contract Manufacturing Organisations (CMOs), you will contribute to ensure the market supply of our products. Process transfers, validations, and optimisation projects at CMOs can also be part of your tasks. Furthermore, you will engage in cross-organisational groups and generate or update relevant technical documentation at the right scientific level. Additionally, you actively contribute to process optimisation, providing scientific input for change requests and deviations, including regulatory document update, authorship, and review. Qualifications We are interested in finding a highly adaptable professional with analytical, innovative, and collaborative skills, which can be used with internal and external stakeholders. You have to excel independently and within diverse teams, ensuring timely and practical solutions across multiple disciplines and external partnerships while also possessing the ability to take decisions. Here are the qualifications we consider essential for this role:

M.Sc. or PhD in synthetic organic chemistry

Experience with organic synthesis. Knowledge with chemical modification of peptides can be an advantage

Fluent in spoken and written English

While not mandatory, it is advantageous to have expertise in process chemistry, specifically in scaling up and transferring processes from pilot to facilities as well as between different sites. Additionally, a background in process characterisation and validation within the pharmaceutical industry and experience with cGMP and handling of deviations and change requests in pharmaceutical settings is an advantage. Applicants without this experience are though still recommended to apply for the position. About the department In the Product Supply (PS) section of Novo Nordisk we manufacture the pharmaceutical backbone of our many quality APIs. PS API Process Support is part of Manufacturing Development and we have six teams responsible for the timely support of the many processes that create our APIs. You can look forward to becoming part of a dynamic, well-functioning, and cross functional team, consisting of 12 scientists, 1 laboratory technician, and 3 other functions. We thrive on professional challenges and work independently with great individual responsibility and a high level of commitment. We collaborate with various stakeholders in the organisation including production departments, analytical departments, CMC, regulatory affairs, and QA. We therefore enjoy being part of a wide range of activities and projects within the organisation. We also have external collaboration with CMOs, which are main stakeholders for this position. Our department is located in Bagsværd, which will be your primary location, but we also have offices in Kalundborg. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We are a dynamic company in an even more dynamic industry and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we are all working to move the needle on patient care. Contact For further information, please contact Hiring Manager, Casper Mørck at +45 3079 8657. Deadline 2 January 2024 Applications are reviewed regularly, so please submit your application 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 process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all job applicants. 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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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 13.12.2023, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.

Type: Øvrige
Sted: Bagsværd

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5. juni 2024	69