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Senior scientist with expertise in raw materials for GMP Production

  • manufacturing
  • Denmark - Hillerød

Are you passionate about using your chemistry skills to understand and ensure the right quality of the raw materials we use in Novo Nordisk? Would you like to contribute to securing suitable suppliers and establishing the right control strategy for our raw materials and thereby contribute to secure the product's safety? If yes, you may be our new Senior GMP Material Scientist in Material Manufacturing Development (ManDev).

About the department
You will join Material ManDev in Product Supply, Sourcing Operations, which consists of 50 employees organised in four teams. A Material Transfer & Management team, two Analytical support teams, and a Project Office. The Senior GMP Material Scientist will be a member of the Material Transfer & Management team responsible for coordinating transfer of raw materials from development to production, and lifecycle activities for existing raw materials. We cooperate with a variety of functions, including other manufacturing development areas, regulatory affairs, development, Suppliers, Quality Control (QC) and Quality Assurance (QA) for raw materials, and various Novo Nordisk production sites and external contract manufacturers.

The position
As our new Senior GMP Material Scientist, your main task will be to contribute with scientific knowledge in the selection of new suppliers for raw materials. You will also be a key driver in setting the control strategy for all the raw materials we use in the Active Pharmaceutical Ingredient (API) and Drug Product (DP) production, when new raw materials are transferred from development and during life cycle management. This requires that you understand the requirements for implementation of GMP Materials used in pharmaceutical production; hence practical experience with pharmaceutical production is an advantage. As Senior GMP Material Scientist, your daily tasks involve solving requests and questions regarding specific raw materials and supporting the processes related to establishment, update, maintenance and discontinuation of GMP Materials. You will become member or driver of relevant cross functional fora. In particular, you will have a close and constructive collaboration with API and DP raw material specialists from development and Manufacturing Support areas. You will have the opportunity to travel at approximately 10 days a year when our raw materials suppliers are to be evaluated.

Qualifications
You have a Master’s degree in Chemistry e.g. MSc.Pharm, MSc.scient or Msc.polyt, or a PHD. You have several years of experience within pharmaceutical production or within organic & protein chemistry combined with a high GMP and compliance mind-set. Furthermore, it is important that you have good project management skills and are motivated by working in the cross field of raw materials and modern production of high quality pharmaceutical products. You have a high level of energy that drives you and inspires your colleagues to deliver on your deadlines and milestones. You thrive in a changing and dynamic work environment and in a job that requires that you contribute to defining your own role and processes that can support an effective flow of projects.

Additionally, you are a true team player who enjoys working in close collaboration with colleagues and stakeholders across functions and departments, and you contribute to the team’s common motivation with a positive, forthcoming attitude.

Lastly, you must have good communication skills and are fluent in both spoken and written English.

Working at Novo Nordisk
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Bodil Rindel at +45 3079 4379.

Deadline
15 February 2018.


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