Lead Validation Specialist – GMP CSV

RoslinCT; City of Edinburgh; On-site; GBP 40,000 - 60,000; Full time

Job summary

A cell and gene therapy company in Scotland is seeking a Validation Supervisor to supervise a team involved in Computer System Validation (CSV). The role includes overseeing quality documentation, monitoring project milestones, and providing expertise during audits. Applicants should have a degree in Life Sciences or Computer Science and experience in a GMP environment. This is an exciting opportunity to make a significant impact in a rapidly expanding company.

Benefits

Generous salary package

31 days annual leave plus 4 public holidays

Competitive pension scheme

Private healthcare

Flexible benefits

Qualifications

• Proven experience in Computer System Validation within a GMP regulated environment.
• Previous background in supervising or leading teams.
• Demonstrable experience of project‑based work, including regulatory audits.

Responsibilities

• Supervise a team undertaking CSV activities for the business.
• Complete quality related documentation in accordance with GMP and SOPs.
• Monitor and report on key milestones within CSV projects.

Skills

Computer System Validation

Leadership

Attention to detail

Project management

IT skills (Microsoft Word & Excel)

Communication skills

Education

Degree in Life Sciences or Computer Science

Job description

A cell and gene therapy company in Scotland is seeking a Validation Supervisor to supervise a team involved in Computer System Validation (CSV). The role includes overseeing quality documentation, monitoring project milestones, and providing expertise during audits. Applicants should have a degree in Life Sciences or Computer Science and experience in a GMP environment. This is an exciting opportunity to make a significant impact in a rapidly expanding company.