CSV Specialist – Catalent
đź“Ť Brussels, 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:
1. Olivia Braszko, TA Specialist at Nalys, will review your application and schedule an initial screening
2. A second interview will be held with one of our technical experts
3. 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!