Clinical Supplies Development Project Coordinator

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Måløv

Are you motivated by challenges and working in a dynamic and diverse environment? Do you have the interpersonal skills to navigate in a complex stakeholder landscape? Do you get motivated by challenges and are you looking for an exciting opportunity to lead critical projects and develop cross-functional solutions? Then we’d like to hear from you. Apply now and join us for a life-changing career! The position As our new Clinical Supplies Development Process Coordinator, you will be responsible for manage both cross-functional projects across several departments and sometimes CVP areas and with different complexity level. The main drivers for the projects you lead is to adapt new processes to Clinical Supplies standards and projects that helps develop the new department Clinical Supplies Development. It will not be investment projects, but projects that require heavy stakeholder engagement and a solid understanding of Clinical Supplies processes. Your main responsibilities and roles will include:

Responsibility of multiple projects/tasks and lead the projects from idea phase to implement phase. This will include collaboration with various stakeholders in all Novo Nordisk and on many organisational levels

Facilitate and drive projects and you should not be the specialist of the processes however you should have knowledge and be interested to go into details and to learn the process further

Successfully deliver solutions to key challenges across Clinical Supplies by excellent project execution. In the work with the projects, you will always collaborate with one or mere subject matter expert and when needed QA

Make independent decisions regarding development of process in both department and corporate level

Thus, a part of the role will include interacting with internal and external stakeholders at high level. Overall, you will be identifying and establishing improvement opportunities in project execution, thereby deliver successful result of development and deployment of standards. Qualifications To succeed in this role, we expect you to have:

A master’s degree in Engineering/Chemistry/Pharmacy or similar

3+ years of experience with Projects Management

Multiple of relevant business experience such as cLEAN®, Six Sigma in business strategy implementation, communication and presentation skills for top management or cross organisational network

Fluency in English both written and spoken

As a person you are excellent at interacting with stakeholders from different cultures and organisational levels and have competencies like strong planning skills, structured, ability to take charge of a group and collaborate with people across boundaries. We are looking for someone inspiring and motivating, a strong innovator, that shrives for continuous improvement, and you have a proven stakeholder and project management track record that excels. You enjoy leading projects and take up responsibility as well as being able to succeed when working both with a team and independently. About the department Our department Clinical Supplies Development is a newly established department and is a part of Clinical Supplies in CMC Development and is based in Denmark, Måløv. Clinical Supplies is responsible for delivering drugs for Novo Nordisk’s clinical trials around the world. In Clinical Supplies, we ensure trial products on time, in the right quality and quantity for all clinical trials conducted by Novo Nordisk. Clinical Supplies Development is responsible for taking new projects and products that has not been running in Clinical Supplies before and make the different needed processes and task operational which will enable a successful business throughout the Clinical Supplies chain. 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. Contact For further information, please contact Director Laila Baadsgaard, +45 3079 9793. Deadline 15 August 2023. Please note that interviews will be carried o.ut an ongoing basis. Please include a cover letter that specifies your motivation for the job. 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 "Administrativ medarbejder", og befinder sig i kategorien "Kontor, handel og service".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 12.7.2023, 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.

Type: Administrativ medarbejder
Sted: Måløv

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