Are you looking for a dynamic and challenging management role within Clinical Compliance in R&D Quality, where you can use your skills with People and Resource management in a highly professional and engaged global environment? If so, we have the perfect opportunity for you to join our management team in Clinical Quality!
Apply now and join a great area where focus is on collaboration, individual development, and proactive clinical quality support to our stakeholders globally.
The position
As our new Manager in R&D Quality in our Clinical Compliance Department, you will support the development area in many aspects of clinical quality. Your primary responsibility is to be accountable for team performance and results.
Your main responsibilities will be focused on:
You will be part of a dynamic management team and will lead employees both in Europa and US East Coast. The position is based in Søborg, Denmark. 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:
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:
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!
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