Analytical Chemist for outsourced materials

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Hillerød

Are you passionate by analytical tasks within chemistry? Do you have a strong knowledge of pharmacopoeia regulations and/or chromatography? Would you like to work in direct contact with external companies? Then apply today as you might be the Analytical Chemist for outsourced materials we are looking for to join our Material Manufacturing Development team! You can look forward to an exciting job in an environment focus on human being and where we seek to be the best in class in everything we do. The position As Analytical Chemist for outsourced materials you will be responsible for:
  • Supporting transfers of analytical methods to Contract Manufacturing Organizations (CMO) for the analysis of raw materials for Good Manufacturing Practice (GMP)
  • Coordinating the implementation of analyses of CMO-produced materials and intermediate or Active Pharmaceutical Ingredient (API) starting materials
  • Reviewing and approving analytical and process validation documentation, as well as writing regulatory documentation related to the analysis of CMO-produced material
  • Cooperating with development in late-phase projects from Phase 2 and onwards (e.g., setting the direction for analytical methods needed for the market)
  • Participating as Quality Control (QC) responsible in internal and external project teams.
    • You will also be involved in the diverse QC assignments we deliver to other parts of Novo Nordisk. This will give you a variety of challenges, and therefore strong collaboration with your colleagues will be essential. You will be part of a team where ideas, problems and solutions are discussed in an open and positive atmosphere. You can work either from Hillerød or Bagsværd, and some international traveling will be expected. Qualifications To be successful in this role we require that you have:
  • A Master´s Degree in Chemistry, Biochemistry, Pharmacy, Engineering, or another relevant field within natural sciences
  • A strong knowledge of GMP obtained within the pharmaceutical or medical devices industry as well as International Conference on Harmonization (ICH)guidelines, and pharmacopoeia requirements
  • A practical background within QC analytical methods within High Pressure/Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Karl Fischer (KF) for raw materials, API and/or drug products
  • Fluency in both written and spoken English.
    • It would be considered as an advantage if you have a previous experience working with CMO. As a person, you will thrive in this position if you enjoy working in project groups and have a high level of energy to drive yourself and your colleagues forward to deliver on milestones. You work in a structured manner and find solutions that are robust and will ensure the correct quality level. You motivate your colleagues with a positive, diplomatic, and forthcoming attitude. You are proactive and you enjoy working independently and representing a group of people. Last but not least, you are a problem-solver, and have a good eye for processes and optimization. About the department You will join Material Manufacturing Development in Product Supply Sourcing Operations. We consist of 100 employees, located in Hillerød and Bagsværd. We are responsible for development and implementation of complex materials (raw materials, excipients, Primary Packaging materials etc.) from development to production at all Novo Nordisk sites. You will join our Analytical support team, which is responsible for the implementation of chromatographic methods, coordination of analyses, and registration for raw materials and excipients, at all Novo Nordisk sites. We cooperate with a variety of functions, including development, Warehouses, Quality Control and Quality Assurance as well as Novo Nordisk sites and CMOs all over the world. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact For further information, you can contact Associate Manager Christina Johansen +45 30776056. Deadline 20 August 2023. Please note that applications will be reviewed and interviews will be scheduled on an ongoing basis. Therefore, we encourage all interested candidates to apply for the position 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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    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Hillerød.

    Jobbet er oprettet på vores service den 2.6.2023, men kan have været deaktiveret og genaktiveret igen.

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