About this role
Role Overview
- Serve as the technical reference for the products, processes and equipment for which you will be responsible
- Learn and master the principles of pharmaceutical qualification and validation
- Contribute to writing URS (User Requirement Specifications) and specifications, ensuring they comply with Novo Nordisk standards and user needs
- Carry out and lead risk analyses to ensure that equipment, processes and systems meet requirements and that relevant testing is conducted during commissioning and qualification
- Review design documents and test protocols provided by suppliers, ensuring they meet our requirements
- Coordinate and support various tests during commissioning and qualification, working closely with stakeholders
- Investigate technical or quality issues, propose corrective and preventive actions, and ensure root causes are addressed to prevent recurrence
- Propose improvements to project and production practices
- Contribute to drafting Standard Operating Procedures (SOPs) and provide the necessary information
- Communicate effectively and persuasively in an international context
Requirements
- Be enrolled in the final year of a Master’s program (M2), an engineering program, or a dual pharmacy/engineering degree
- Excellent spoken and written English (very strong level required)
- Prior industrial experience gained through an internship or work-study (alternance)
- Knowledge of manufacturing, ideally in the pharmaceutical sector, and experience working in a cGMP environment
Benefits
- Multicultural environment
- Challenging technical projects
- Genuine opportunities for professional development