Back to Job SearchWe are currently looking for a CSV Lead to join a leading Pharmaceutical company in the Walloon Region, Belgium. This is an opportunity to play a pivotal role in the digitalization of CSV processes through the implementation of innovative systems. The role offers an excellent chance for a senior professional to lead process improvements and ensure compliance within a dynamic project environment.
In this position, you will work closely with cross-functional teams, including project managers, system owners, developers, and validation SMEs, to enhance and automate CSV governance workflows. This is an ideal opportunity for someone looking to impact the future of validation processes within a global organisation.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the CSV Lead will be varied, however, the key duties and responsibilities are as follows:
- As the CSV Lead you will oversee the digitalization of CSV governance processes by translating validation workflows into digital systems and ensuring compliance with regulatory standards
- As the CSV Lead you will collaborate with project teams to review requirements, provide validation support, and contribute to system validation activities
- As the CSV Lead you will Challenge existing validation workflows to identify opportunities for process efficiency and improvement
- As the CSV Lead you will Support system validation activities, ensuring documentation and procedures meet internal and external standards
- As the CSV Lead you will act as a strategic partner, influencing validation practices and driving continuous improvement initiatives
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the CSV Governance Lead we are looking to identify the following on your profile and past history:
- Degree or higher level in a relevant field (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management)
- Proven extensive experience (5+ years) in Computer System Validation within the life sciences sector, demonstrating autonomy and decision-making capability
- Strong understanding of CSV governance, validation processes, and regulatory compliance
- Ability to translate complex business requirements into system specifications and validation protocols
Key Words: CSV / Validation / Digitalization / Systems / Governance / Compliance / Project Management / Veeva / Process Improvement / Life Sciences / Pharmaceutical / Validation System / Computer Systems Validation / Pharma / Pharmaceutical / Walloon Region / Wallonie
"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."
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.
