Are you motivated by executing strategic projects with many stakeholders? Do you see yourself working in the interface between supply chain processes, automation, and IT? And are you comfortable taking responsibility and making things happen? Then you might be the right person to take on the role as Project Manager in CMC Clinical Supplies.
The position
The pipeline of clinical trials is increasing both in volume and types, and in Clinical Supplies we need to adapt to these changes. We also want to continuously improve the clinical supply chain and we do this through projects anchored in our masterplan. As our new Project Manager, you will be responsible for executing a broad range of projects with a focus on Automation, IT & Digitalisation, applied to supply chain processes. As Project Manager you will be deeply involved in the solutions of the project, so you need to be curious and willing to go into details when needed.
As part of Supply Chain Optimisation, you will:
Lead our strategic projects with stakeholders across the business unit often anchored with a steering group.
Ensure alignment with the business strategy.
Work very independently, but with involvement of colleagues in Clinical Supplies at all levels including CS Management, CS Associate Managers as well as colleagues in the business area.
Challenge our vendors when the projects include external vendors.
You will get in-depth understanding of our processes and how they are linked across the clinical supply chain as well as backwards towards production facilities in CMC and use this in the projects. You will also be a resource for colleagues with less experience and to whom you may direct work.
Qualifications
To thrive in this role, you:
Hold a master’s degree in supply chain, engineering, economics, or a related field, with over 5 years of solid project management experience.
Alternatively, you have a strong background in supply chain, IT, and automation, with a talent for organizing and driving initiatives that you wish to develop further as a Project Manager.
Ideally, you have supply chain experience
It would be considered as a plus if you understand regulatory requirements ideally from the pharmaceutical industry.
On a personal level, you are structured, thrive in delivering results, and possess excellent communication skills. You naturally connect with colleagues at all levels of the organization, have a strong flair for stakeholder management, and are fluent in both written and spoken English.
About the department
Before drug is approved for market use, drug candidates are tested in clinical trials. CS 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 highly engaged and dedicated professionals, who work across CS and with direct link to CS Management. Our role is to carry out strategic projects 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 and productivity and agility improvements. In recent years, a large number of improvement projects and initiatives has been carried out successfully in the business area. The main focus has been automation and digitalisation, and our ambition is to become fully digitalised.
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