Senior Manager for Clinical Supplies Development
3 days ago
The position
The department CS Development consists of about 15 employees, responsible for setting up new processes to handle what is needed to bring clinical supplies to clinical trials all over the world. We are a part of Chemistry, Manufacturing and Control (CMC) Clinical Supplies. CMC Clinical Supplies is a complete value chain from production to shipments to patients globally.
As Associate Manager for CS Development, you will work closely together with the Director and create the perfect environment for your team. Your team consists of 8-10 employees that both handle projects to support that CMC Clinical Supplies is fit to run trials, but also have the responsibility of support processes that ensures that CMC Clinical Supplies can operate when using new products, e.g. new ways of handling secondary packing, blinding set up and much more.
You will be responsible for setting up the structure for the team in line with our strategy and in a way where we can operate with focus on simplicity and productivity. We are a dynamic development environment, where sharp priorities are needed every day to reach more patients in the future.
Key Responsibilities- Set direction for the team both short and long term to ensure that all activities are planned and completed timely and in compliance with GMP/GCP standards.
- Maintain a high level of drive and commitment in the team, through visible and authentic leadership.
- Develop a culture where everyone is ready to challenge status quo, feel safe to speak up and where diversity of different thinking is appreciated.
- Focus on stakeholder interaction and alignment is needed.
- You hold a MSc or other degree in a relevant field (e.g. engineering, supply chain, pharmacy).
- You have several years of experience in people management, ideally within a development or production environment.
- You have solid knowledge of pharmaceutical industry, Good Manufacturing Practice (GMP) and/or Good Clinical Practice (GCP).
- You are familiar with various LEAN principles.
- You have strong communication skills in Danish and English, both written and spoken.
As part of Novo Nordisk PSQIT organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a "can do" mind-set.
Clinical Supplies Development is a part of Clinical Supplies in CMC Development & Scaling. CMC Clinical Supplies are responsible for ensuring that labelled and packed clinical trial products are available on time, in right quality and quantity for all clinical trials conducted by Novo Nordisk.
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