Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409
General information Publication date 02/08/2026 Position description Category OPERATIONS - CONSULTING Job title CSV Engineer - Life Sciences - M/F/X Contract Permanent contract Job description About the role This role involves ensuring compliance with cGMP standards
Your Role As a Computer System Validation (CSV) Engineer, you will play a key role in ensuring that computerized systems used in regulated environments meet compliance standards and operate as intended. You will collaborate with cross-functional teams to develop
Make your mark for patients To strengthen our Bio DS Quality we are looking for a talented profile to fill the position of: Bio DS Quality CS Manager – Braine l’Alleud, Belgium. About the role You
Make your mark for patients To strengthen our Bio DS Quality we are looking for a talented profile to fill the position of: CSQA and Data Integrity Specialist – Braine l’Alleud, Belgium. About the role The
Make your mark for patients We are looking for a Digital Technology Lab Technology & Operations Specialist who is proactive, solution-oriented, and collaborative to join our Digital Technology Patient Solutions team, based in our office in
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
As part of our Life Sciences activities, we are looking for a CSV Validation Engineer (PAS-X) to support the implementation, validation and compliance of computerized systems within highly regulated pharmaceutical manufacturing environments. You will play a key role
Functieomschrijving Jouw rol als CSV Validation Engineer Als CSV Validation Engineer sta je in voor het valideren van geautomatiseerde systemen binnen een farmaceutische omgeving, zodat ze voldoen aan alle kwaliteits- en compliancevereisten. Je draagt bij aan
Your responsibilities include: - Carrying out preventive maintenance according to the CMMS plan (Computerized Maintenance Management System). - Quickly and efficiently detecting and resolving technical faults. - Making technical improvement proposals based on your experience with breakdowns. -