Back to Job SearchWe are recruiting a Computer System Validation (CSV) Engineer to join a leading Pharmaceutical in the Walloon Region, Belgium. As the CSV Engineer, you will play a pivotal role in ensuring the integrity and compliance of computerized systems within the organisation.
This is a mission until the end of April 2026 with possible extension.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CSV Engineer will be varied however the key duties and responsibilities are as follows:
1. As the CSV Engineer, you will be performing routine and project activities with the team, managing full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated, and retired in compliance with GxP regulation and CSV procedure.
2. As the CSV Engineer, you will be validating manufacturing, laboratory, and other business systems, working with project teams to compile user requirements (URS) for local systems, and writing validation plan deliverables such as Functional, Data Integrity and Audit Trail Risk Assessments, Test Protocols, test scripts and Reports (IQ, OQ, PQ), Traceability Matrix, and Validation Summary Report.
3. As the CSV Engineer, you will be executing the test Protocols (IQ, OQ) and participating in Performance Qualification (PQ) ensuring that the appropriate documentation of testing is performed, and executing periodic reviews throughout system lifecycles to ensure systems are maintained in a validated state during their operational life.
4. As the CSV Engineer, you will be writing Computerized Systems Administration Work Instructions, Computerized Systems Audit Trail Logbook, working with system vendors to leverage appropriate information and documentation into CSV activities, and compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CSV Engineer we are looking to identify the following on your profile and past history:
1. Relevant degree in a life science subject.
2. Proven industry experience in CSV in Pharma/Biologics.
3. A working knowledge and practical experience with GxP regulations and CSV procedures.
Key Words: CSV Engineer / Computer System Validation / GxP / Life Sciences / Belgium / Validation Engineer / CSV Documentation / System Lifecycle / Compliance / Data Integrity / Test Protocols / Audit Trail
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
This is a mission until the end of April 2026 with possible extension.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the CSV Engineer will be varied however the key duties and responsibilities are as follows:
1. As the CSV Engineer, you will be performing routine and project activities with the team, managing full lifecycle validation for all applicable computerized systems, ensuring they are designed, validated, operated, and retired in compliance with GxP regulation and CSV procedure.
2. As the CSV Engineer, you will be validating manufacturing, laboratory, and other business systems, working with project teams to compile user requirements (URS) for local systems, and writing validation plan deliverables such as Functional, Data Integrity and Audit Trail Risk Assessments, Test Protocols, test scripts and Reports (IQ, OQ, PQ), Traceability Matrix, and Validation Summary Report.
3. As the CSV Engineer, you will be executing the test Protocols (IQ, OQ) and participating in Performance Qualification (PQ) ensuring that the appropriate documentation of testing is performed, and executing periodic reviews throughout system lifecycles to ensure systems are maintained in a validated state during their operational life.
4. As the CSV Engineer, you will be writing Computerized Systems Administration Work Instructions, Computerized Systems Audit Trail Logbook, working with system vendors to leverage appropriate information and documentation into CSV activities, and compiling and maintaining accurate CSV documentation, ensuring full traceability throughout system lifecycles.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the CSV Engineer we are looking to identify the following on your profile and past history:
1. Relevant degree in a life science subject.
2. Proven industry experience in CSV in Pharma/Biologics.
3. A working knowledge and practical experience with GxP regulations and CSV procedures.
Key Words: CSV Engineer / Computer System Validation / GxP / Life Sciences / Belgium / Validation Engineer / CSV Documentation / System Lifecycle / Compliance / Data Integrity / Test Protocols / Audit Trail
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Your Recruitment Consultant
Share this Job
