Senior QC Analytical Chemist

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Hillerød

Do you enjoy analytical tasks within chemistry and would like to work in direct contact with external companies?

Apply today for a life-changing career as a Senior QC Analytical Chemist in Material Manufacturing Development! You can look forward to an exciting job in an environment where we seek to be the best in class in everything we do.

The position

As a Senior QC Analytical Chemist your primary tasks will include:

  • supporting transfer 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 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:

  • working experience with GMP as a chemist or similar
  • good knowledge of ICHguidelines, and pharmacopoeia requirements
  • strong practical and theoretical background within QC analytical methods will be required, e.g., HPLC, GC, KF for raw materials, Active Pharmaceutical Ingredient (API) and drug products
  • a Master´s Degree in Chemistry, Biochemistry, Pharmacy, Engineering, or another relevant field within natural sciences
  • coordination and CMO experience would be desired, especially within analytical method transfer.

You are proficient in both written and spoken English. It would be an advantage if you also have knowledge of systematic problem-solving, and a good eye for processes and optimization.

As a person, you will thrive in this job 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.

About the department

You will join Material Manufacturing Development in Product Supply Sourcing Operations. We consist of 70 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

At Novo Nordisk, we don’t wait for change. We drive change. We’re 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. 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 to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing.

Contact

For further information, you can contact Associate Manager Christina Johansen

+45 30776056.

Deadline

11 December 2022.

Applications are reviewed on an ongoing basis, so please submit your application as soon as possible. To ensure an efficient and fair 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.

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Information og data

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 9.8.2022, 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.
  • Øvrige
  • Hillerød

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