(Senior) Development Scientist for Raw Material qualification
Novo Nordisk
- Bagsværd, Hovedstaden
- Permanent
- Fuldtid
- Coordination, introduction, qualification and life cycle management of different types of materials (raw materials, consumables, excipients) for GMP production to clinical trials from the entire Novo Nordisk development portfolio e.g. Cell Therapy.
- Ensure that the suitability of materials is properly evaluated based upon the intended use.
- Setting the internal release specification for the warehouse and quality control (QC).
- Close contact and collaboration with various external stakeholders such as material suppliers, logistics services etc., to obtain sufficient knowledge to ensure patient safety, GMP, and GDP compliance.
- GMP experience in the pharmaceutical industry preferably from a similar role
- Coordinating tasks within a large project with many different stakeholders
- Excellent communication skills and proficiency in both spoken and written English
- Great collaboration skills, structured, and have a natural sense of priority and not afraid to set direction.
- A team-player who enjoys cross-functional, cross-departmental and stakeholder collaboration.