Reference Material Coordinator

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Måløv

Are you ready to apply your analytical skills and project management experience in an exciting organization? Do you want to take part in the implementation of new drugs and make a difference in our vision to change the life of patients? And do you want to join a dynamic and highly competent Reference Material team? Then this is your call for action. CMC Drug Product & Analytical Development is looking for a new Reference Material Coordinator. Apply today and join us for a life-changing career. The position As a Reference Material Coordinator you will be responsible of driving the process for developing and establishing our reference materials for all current and future products in the CMC product portfolio. Together with 5 colleagues you will be responsible for coordinating the tasks related to reference materials. Your primary tasks will be to:
  • Coordinate the production and analysis of the reference materials

  • Prepare the supporting documentation

  • Implement and maintain the reference materials

  • Support the internal users of reference materials at Novo Nordisk.

    • Furthermore, as a part of your job, you will:
  • Develop the reference material strategy as part of the overall analytical strategy for each project

  • Prepare regulatory documentation for various authorities and answer questions to the documentation

  • Transfer the know-how to the corresponding support function in Product Supply when the products enter the market.

    • You will be a part of a small group that is well structured and pursues solid results through good collaboration. Your daily work will have you working broadly across the organisation, including interactions with relevant analytical laboratories, scientists, project managers, statisticians, and QA. You will be part of at RM network across Novo Nordisk. Finally, you will join a harmonious team and department with competent, caring, and positive colleagues. Qualifications You will be a great asset to our team because you have:
  • A relevant academic degree, preferably a master’s degree, within Pharmacy, Chemistry, Engineering, or a similar field

  • Solid experience in successfully managing and executing projects in pharmaceutical industry

  • Relevant experience from working with reference materials, analytical development, production, or QC

  • Experience from working with product specifications, analytical methods, production and/or regulatory documentation in the pharmaceutical industry is an advantage

  • Full professional proficiency in English.

    • On a personal level, you enjoy working on long-term projects in implementing new reference materials and processes. You should enjoy taking responsibility, work in an organized way, be visible and finalize projects until fully implemented. You are naturally good at communicating with all types of stakeholders both verbally and in writing. This helps you to keep all your stakeholders aligned, informed, and engaged. You are motivated by the opportunity of getting a large network across the organisation. About the department Your new department, CMC Drug Product & Analytical Development Project Office, consists of 40 employees located in Måløv. The department is involved in early and late-stage drug product development, analytical development, and establishment of reference material of new entities moving through the clinical phases of drug product development. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. 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. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Associate Manager Susie Christensen at +45 30775028 Deadline Apply before October, 17 2023. Applications will be reviewed continuously, and interviews will be conducted during the posing period, so please do not hesitate to apply. 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 Måløv.

    Jobbet er oprettet på vores service den 2.10.2023, men kan have været deaktiveret og genaktiveret igen.

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    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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