Manufacturing Development Scientist

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Gentofte

Are you ready to make a difference for people living with haemophilia and other Rare Diseases? Do you want to work with the development of complex production processes and be part of a super-engaged team? Are you eager to learn about and implement new technologies? Then look at this exiting vacant position as Manufacturing Development Scientist at our Novo Nordisk site in Gentofte. The position
We offer an exciting position where you will be working with many different tasks within the development and support of Biotech and Rare Disease (BRD) manufacturing processes for active pharmaceutical ingredients (APIs). Your focus will be on outsourced productions, working in close collaboration with internal stakeholders and with international contract manufacturing organizations (CMOs) to supply critical raw materials, starting materials, intermediates and bulk API. In this dynamic role you will:
  • Be responsible for key aspects of commercial, cGMP productions such as master formulas, risk management, control strategy, development studies and stability.
  • Be a part of an experienced, cross-functional project team.
  • Get the opportunity to work with a wide range of production technologies such as chromatography, chemical synthesis, filtration, and lyophilisation,
  • Work with transfer of manufacturing processes from late-phase development to commercial launch,
  • Act as a subject-matter expert within projects such as yield and process optimisations,
  • Build and maintain good relations with a wide range of Novo Nordisk stakeholders such as Global Contract Manufacturing, Quality Assurance, Research and Development, Regulatory Affairs and Quality Control.
  • Communication and collaboration skills are of key importance to ensure efficient distribution of tasks and alignment across the team, the department and within BRD. Expect to be on business travels approximately 10 days per year. Qualifications
    To succeed in this position, you have:
  • As a minimum a master’s degree within a scientific field such as engineering, biotechnology, chemistry, biology or similar
  • 2+ years of experience working with manufacturing operations or development
  • Experience with project and stakeholder management
  • Experience in pharmaceutical production and is familiar with GMP and systematic-problem-solving tools such a cLEAN
  • You need to have full professional proficiency in English. As a person, you are outgoing and self-driven. You thrive in an international environment where you get to throw yourself in at the deep end, always seizing an opportunity for personal and professional development. About the department BRD Manufacturing Development & Quality Control has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 460 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio. Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible. Working at BRD, Novo Nordisk
    Biotech & Rare Disease (BRD) is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2500 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we also strive to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career? Contact
    If you have any questions about the job, please do not hesitate to contact Associate Manager Camilla Christensen at [email protected]. Deadline
    February 20th, 2023. Interviews will be conducted on an ongoing basis. 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 to your CV. We commit to an inclusive recruitment process and equality of opportunity for all our 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.


    Information og data

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

    Arbejdsstedet er beliggende i Gentofte.

    Jobbet er oprettet på vores service den 3.2.2023, 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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