Job Description

Ready to take a quality step forward in your professional journey? Would you like to be part of a company offering numerous development opportunities in a multicultural and international environment? Then keep reading to learn more about this opportunity based at our production site in Brussels!

Your New Role

As a CSV Specialist, you will help ensure compliance of computerized systems related to our Brussels production site. Your main responsibilities will include:

• Execute validation projects for production equipment, laboratory automated instruments, and systems, while contributing to the equipment lifecycle (validation, periodic review, implementation).
• Create and support validation deliverables, such as project plans, impact assessments, user requirements, test strategies, risk assessments, protocols, SOPs, periodic reviews, and system decommissioning activities.
• Contribute to remediation and data integrity projects, ensuring compliance with US, EU, and other regulatory requirements, while respecting internal procedures and EHS standards.
• Collaborate with production, IT, and laboratory teams to successfully carry out validation projects and effectively implement the validation program.
• Foster a culture of continuous improvement by identifying areas for process optimization and actively contributing to their implementation.

Your Skills & Qualifications :

• You have a technical or scientific background (bachelor’s or master’s degree).
• You have min 2 years of experience in CSV or equipment qualification, ideally in the pharmaceutical industry.
• You have a solid understanding of computerized systems and an interest in IT.
• You possess knowledge of GMP and associated regulatory requirements.
• You will work in an international environment, so you are able to understand and communicate in English, both verbally and in writing.
• You have excellent interpersonal and communication skills, and you enjoy collaborating effectively in a team setting.
• You are detail-oriented, autonomous, proactive, and organized.

Your New Department

You will join the Qualification Department, under the supervision of the Computerized Systems Validation (CSV) Supervisor, within a dynamic team of 6 skilled professionals.

Working at Novo Nordisk

Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 63,400 employees. Together, we go further. Together, we’re life changing.

Want to know more?

Contact

Apply directly on our website.

Deadline

Kindly apply before 09/02. Applications are reviewed on an ongoing basis.

We are committed to an inclusive recruitment process and equal opportunities for all candidates. We are happy to discuss flexible working arrangements depending on the role and business needs.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.