Alternant Ingénieur Process chez Novo Nordisk, servant de référence technique pour l'industrie pharmaceutique. Apprendre et maîtriser la qualification et validation pharmaceutique.
Responsibilities
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
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