CSV Specialist – Catalent
📍 Brabant Wallon, Belgium
About Nalys
Nalys is a fast-growing consultancy company specialized in high-tech engineering and life sciences. We partner with leading organizations to deliver innovative solutions and expert support across a wide range of technical domains. At Nalys, we combine deep expertise with a human-centric approach — empowering our consultants to thrive and our clients to succeed. Joining Nalys means becoming part of a collaborative, agile, and forward-thinking team that values excellence, innovation, and continuous growth.
The Role & Responsibilities
As a CSV Specialist, you will play a key role in ensuring compliance and integrity of computerized systems within a leading pharmaceutical environment. Your responsibilities will include:
* Validation Projects: Execute validation activities for process equipment, laboratory instruments, and computerized systems in line with different specific guidelines
* Validation Deliverables: Prepare and maintain documentation such as project plans, user requirements, risk assessments, test protocols, SOPs, and periodic reviews
* Regulatory Compliance: Ensure adherence to US regulations, and other relevant regulations, as well as EHS requirements
* Collaboration & Continuous Improvement: Work closely with manufacturing, IT, and laboratory teams to implement validation programs and foster a culture of continuous improvement.
Skills & Qualifications
* You hold a Bachelor’s or Master’s degree in Computer Science, STEM, or related scientific field
* You have a strong knowledge of CSV and IT regulations
* You are familiar with GMP systems and Excel validation workflows
* You understand Project Management and Software Development Life Cycles
* Excellent communication, leadership, and problem-solving skills
* You are able to work independently and manage multiple priorities under strict deadlines.
The recruitment process
At Nalys, our hiring process is designed to be transparent and engaging:
* Olivia Braszko, TA Specialist at Nalys, will review your application and schedule an initial screening
* A second interview will be held with one of our technical experts
* Final interview with our Business Unit Director, Jimmy Rousseaux.
If you’re passionate about compliance and want to contribute to the success of a global pharmaceutical leader, we’d love to hear from you!