Associate Manager

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Do you enjoy developing people to achieve great results? Are you motivated by optimising business processes through IT? Would you like to shape how we develop IT in the future?

If so, you could be our new Associate Manager for IT Development in Clinical Supplies. Read on to find out more! The Position As our new Associate Manager, you will be responsible for a newly established team of eight employees. The team consists of Product Owners, System Developers, IT Process Engineers and a Data Engineer. The team drives and develops IT systems and tools supporting the processes in Clinical Supplies and supports Clinical Supplies with business data. The team is part of the department Supply Chain Optimisation working across Clinical Supplies. We have a vision of becoming fully hands-off in our processes, and therefore, we continuously develop our system landscape. IT Development is responsible for internally developed tools and systems as well as our new MES system used by employees across Clinical Supplies. Your responsibilities will include:
  • Setting the direction for the team both in the short run and the long term to ensure that we develop our systems and tools in the optimal way.
  • Professionalising IT development in Clinical Supplies.
  • Developing the IT architecture in Clinical Supplies including product visions and roadmaps for solutions and consistency across solutions.
  • Excellent stakeholder management and collaboration with Line of Business as well as external vendors.
  • You maintain a high level of drive and commitment, and, through visible leadership and sparring, you develop a culture where everyone is ready to challenge systems and processes and continuously make them better, smarter, and faster. As Associate Manager in Supply Chain Optimisation you will be reporting to the Director of Supply Chain Optimisation and be part of the Supply Chain Optimisation management team. Qualifications To succeed in this role, you have:
  • A Master’s degree in IT, Engineering, Supply Chain Management, Economics or similar and have 5+ years of relevant experience.
  • Experience in people or project management, supporting business processes with IT solutions.
  • Experience in IT development including SAFe and agile principles and tools.
  • Collaborated and built relations with stakeholders cross-functionally.
  • Ideally, 3-5 years of experience within the pharmaceutical industry, health authority requirements, good knowledge of Good Manufacturing Practice (GMP).
  • An interest in planning and supply chain management processes is considered advantageous.
  • You have a proven ability to inspire and motivate others, a structured approach to your work and the ability to set the scene and give direction and drive to empower a team to deliver high quality results. As a person, you are a team player and find motivation when reaching common goals. About the Department Before drug is approved for market use, drug candidates are tested in clinical trials. Clinical Supplies is responsible for delivering drugs for Novo Nordisk’s clinical trials around the world. Our tasks range from receival of the clinical protocol to final delivery of clinical product at site, which include planning, drug product filling, labelling, packaging and shipping of product. Hence, our processes include many different steps and hand overs. Supply Chain Optimisation is a department of 20 colleagues, who work across Clinical Supplies and with direct link to management in Clinical Supplies. We are divided in Business Development and IT Development. Our role is to carry out strategic initiatives optimising the clinical supply chain. Our way of working is informal and ambitious at the same time. We work in close cooperation with Line of Business. We are responsible for optimisation of the clinical supply chain, and our focus is lead time reduction as well as productivity and agility improvements. In recent years, many improvement projects and initiatives have been carried out. The main focus has been automation and digitalisation, and our ambition is to become fully digitalised. 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 Eva Willumsen (Director, Supply Chain Optimisation) on: +45 3079 4101. Deadline Apply before January 29, 2023. 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.


    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 6.1.2023, 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.
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