Project Manager for Improvement Projects
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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. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing. Contact For further information, please contact Associate Manager Luca Elianti at [email protected] (there might be delays due to the holiday season) or get to know us better by visiting www.novonordisk.com/careers. Deadline 27 July 2024 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 "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 11.7.2024, 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.
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