Supply Chain Planner
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Are you ready to take on the responsibility of ensuring timely and adequate trial products for clinical trials? Do you thrive in a dynamic environment where you can drive process optimization and contribute to the success of bringing new drugs to market? If so, we have an exciting opportunity for you to join our Supply Chain Planning team at Novo Nordisk. Apply today for a life-changing career! The Position As a Supply Chain Planner, you are responsible for the Clinical Supply chain ensuring timely and adequate trial product for clinical trials. This translates into the following tasks: Efficient planning of trial product which needs to be packed and distributed using forecasting and planning tools Get in depth understanding of our products how set-up impact the clinical supply processes Constant dialogue with colleagues within our own area and end customers in other parts of Novo Nordisk Ability to drive process optimisation and projects across several areas. The job entails stakeholder management, and you are responsible for timely and adequate information to stakeholders locally and globally during trial conduct.
You are expected to contribute to identifying and proactively engage in implementing standardization, optimization, and simplification of processes. The tasks in this job role requires a quality mindset. Qualifications To succeed in this role, you have: A bachelor’s or master’s degree within life sciences (e.g., pharmacy) 2-4 years GMP experience Excellent computer skills and you can handle several IT systems in daily operation Experience with process optimization and LEAN tools Fluency in written and spoken English. You are great at engaging and managing stakeholders and are able to see continuous improvements as a natural part of your job. You are analytical, structured and can thrive work with frequently changing priorities and tight deadlines. About the Department Supply Chain Planning (SCP) is a key member of CMC Development and scaling, Clinical Supplies (CS) and is vital in bringing new drugs to market. Our responsibility is to ensure that trial products are available on time and in the right quality and quantity for all clinical trials conducted globally by Novo Nordisk. We operate in the combined field of supply chain management and regulatory requirements within drug 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 Christina Petersen Engmose, +45 30757564 Deadline Apply before 28 January 2024. Applications will be screened on an ongoing basis, so you are encouraged to apply 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.
You are expected to contribute to identifying and proactively engage in implementing standardization, optimization, and simplification of processes. The tasks in this job role requires a quality mindset. Qualifications To succeed in this role, you have:
Information og data
Denne ledige stilling har jobtypen "Supply Chain Management", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 12.1.2024, 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.
- Supply Chain Management
- Måløv
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| 12. juni 2024 | 2 |
| 11. juni 2024 | 3 |
| 10. juni 2024 | 3 |
| 9. juni 2024 | 3 |
| 8. juni 2024 | 3 |
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| 16. maj 2024 | 1 |
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| 13. maj 2024 | 1 |