Drug Product Scientist for CMO collaborations
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Måløv
Do you have what it takes to break new land and develop injectable biopharmaceutical products during clinical development? Are you eager to act in a team linking research and Contract Manufacturing Organisation (CMO) Drug Product production during clinical development? If yes, then apply now. The Position As our new Scientist, you will have the responsibility for product and process development to secure optimal pharmaceutical characteristics and stability. The open position is in the early phase team where the primary focus will be formulation and CMO productions during clinical phase 1-2. Your responsibilities will include: Working in close collaboration with a project team, and be responsible for designing, interpreting, and reporting studies on drug products
Project responsible for Technology Transfer to external CMOs for phase 1-2 productions. The responsibility will cover transfer of the Drug Product formulation and the manufacturing process
Writing documentation for internal and external use including clinical trial applications and patent applications
Interacting with a wide variety of internal stakeholders, e.g., CMOs, Global Research, Regulatory affairs, Quality Assurance and Analytical Development
In the team you will set a clear scientific direction and inspire your colleagues with your positive can-do attitude. The position is expected to require a limited amount of travel activities. Qualifications To succeed in this role, you have: A PhD or a Master’s degree within Pharmacy, Chemistry, Biophysics, Engineering or similar of related field of study, preferably backed by working experience within drug product development and/or production
Experience within CMO activities is considered an advantage
Experience in formulation and/or process development and documentation, including regulatory and quality aspects of drug development projects
Ability to promote collaboration with other parts of the organisation and CMOs as the position requires close interaction with a variety of stakeholders
Possess strong communication skills both verbally and written in English
We are looking for someone who can show drive and have a positive can-do mind-set. You enjoy working in a team with highly motivated people dedicated to developing the next generation of pharmaceuticals in a continuously developing environment. At the same time, you should work systematically, and you can adhere to strict documentation and quality standards. You have excellent collaborative skills, and agility and flexibility are a natural part of your approach to interact with colleagues in the department and with your stakeholders. About the Department Injectable Formulation Development is part of CMC Development & Scaling. We are responsible for developing formulations and production processes for injectables of new biopharmaceutical products. The department is organised in 4 teams and we are approximately 80 employees in total. The department is situated in Måløv, Denmark. In our daily work we link research and pilot production and drive the entire portfolio of injectable projects from early stage (phase 1-2) to late-stage (phase 3-submission) development. The development portfolio in the department include all injectables projects, e.g. GLP-1 products, insulins, monoclonal antibodies, and oligonucleotides. 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 Senior Manager Andreas van Maarschalkerweerd at +45 3075 4300. Deadline Apply before January, 10 2024. Applications will be reviewed 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 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.
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 23.10.2023, 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.
- Øvrige
- Måløv
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