Manager in R&D Quality - Søborg, Danmark - Novo Nordisk

Beskrivelse

The position

offers high impact, flexibility, and you are expected to take ownership and responsibility for leading the team to successfully setting the right quality level in the global organisation.

Qualifications To be a competitive candidate, you should have:
A master's degree with min.

6-8 years relevant work experience, with a minimum of 3 years leadership experience/informal leadership experience More than 5 years of experience from preferably a quality Good Clinical Practice (GCP) position or alternatively a position involving planning and conduct of global clinical trials Solid GCP experience to drive the decisions, strategies and support your employees It is an advantage if you have experience from working in a project oriented, international matrix organisation and from cross-organisational work You have a positive and pragmatic approach to problem solving.

You are proactive, courageous and have strong communication and interpersonal skills. You thrive with people management, are organised, quality conscious as well as curious by nature. You are a team player, and you thrive working across departments in an international organisation.

About the department Clinical Compliance is one of four departments in the area Clinical Quality, which is part of R&D Quality at Novo Nordisk.

We play a vital role in supporting the drug development process to ensure high quality as well as fit-for-purpose processes.

In Novo Nordisk, we have an ambitious drug development program, where we work in a global setting with focus on delivering viable products that make a difference to patients and ultimately benefit society.

In the Clinical Compliance Department, we support the development organization and drive several activities within strategic areas:

Clinical Quality Partners for our stakeholders globally GCP Advice Squad – a global support function Clinical Quality and Compliance oversight Clinical Quality and Compliance activities supporting integrations of Novo Nordisk acquired companies and partnerships We also take active part in cross organizational improvement projects and provide general quality & compliance support to our global organisation.

We support with tasks across Clinical Quality such as support during inspections, CAPA QA tasks, pre-assessments of new vendors and other clinical quality related tasks.

We are on an exciting journey to bring quality to the top of the agenda throughout the R&D organization – we hope you will join us 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 necessary 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.