Global Manufacturing & Supply
Brussels, Belgium
Ensure the quality and safety of life‑saving medicines by validating the systems that bring them to patients. Join us during an exciting journey at our Brussels sterile manufacturing!
Your new role
As a CSV Specialist, you will play a critical role in ensuring the regulatory compliance of computerized systems that support our production operations.
Day‑to‑day – Your Tasks Will Include
* Executing validation projects for production equipment, laboratory automated instruments, and computerized systems throughout their lifecycle
* Creating and supporting validation deliverables including project plans, impact assessments, user requirements, test strategies, risk assessments, protocols, SOPs, and periodic reviews
* Contributing to remediation and data integrity projects, ensuring compliance with US, EU, and other international regulatory requirements
* Collaborating with production, IT, and laboratory teams to successfully implement validation programs and drive projects forward
* Fostering a culture of continuous improvement by identifying process optimisation opportunities and actively contributing to their implementation
* Supporting system decommissioning activities and equipment lifecycle reviews
Your new department
In Global Manufacturing & Supply, we cover the full value chain from drug and device development to marketed Novo Nordisk products. We are more than 30,000 colleagues across the globe with the shared responsibility of scaling molecules, processes, devices, and products, dedicated to supplying life‑saving medicines to the patients who need them most.
You’ll be part of the Qualification/Validation Department, working within a dynamic team of skilled CSV professionals under the supervision of our CSV supervisor.
Your Skills & Qualifications
* A technical or scientific background with a bachelor's or master's degree
* Experience in CSV or equipment qualification, ideally gained within the pharmaceutical industry
* A solid understanding of computerized systems and a genuine interest in IT
* Knowledge of GMP and associated regulatory requirements (ideally)
* Strong English language skills, both verbal and written, to work effectively in our international environment
* Excellent interpersonal and communication skills with the ability to collaborate across teams
* A detail‑oriented, autonomous, and proactive approach with strong organisational skills
What We Offer
At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage.
Salary: Annual base salary ranges from 47,190.00 to 75,500.00 EUR, corresponding to the level of the position.
The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.
Incentives and Benefits: The salary package may include short‑term and/or long‑term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.
Learn more about our Reward Philosophy here.
Apply Before: May 13th 2026
#J-18808-Ljbffr