CSV Supervisor I: GMP Systems & Validation Lead

Roslinct Eu; Dalkeith; On-site; GBP 42,000 - 52,000; Full time

Benefits offered by this job

Private healthcare

Cycle2Work

Pension scheme

Life cover

Flexible benefits

Job summary

RoslinCT in the United Kingdom is seeking a Computer Systems Validation (CSV) Supervisor I to join the Validation team. You’ll supervise a small team carrying out CSV activities across facilities management software and equipment software.

You will monitor milestones, ensure documented evidence, and prepare and approve validation documents in line with GMP and SOPs. Strong communication and project-based experience are essential.

Qualifications

• Proven experience in Computer System Validation within a GMP environment.
• Experience supervising or leading teams.
• Experience with regulatory audits, GAP analysis, risk assessments and Data Integrity Assessments.

Responsibilities

• Supervise CSV activities for facilities management software and equipment software.
• Track milestones and ensure documentation at each stage.
• Prepare, review and approve CSV documents such as plans, protocols and reports.
• Coordinate validation schedule for new facilities when required.
• Communicate CSV outcomes with clients and support audits.

Skills

Team leadership

Collaborative work

Project coordination

Education

Life Sciences or Computer Science degree

Tools

Microsoft Word

Microsoft Excel

Job description

RoslinCT in the United Kingdom is seeking a Computer Systems Validation (CSV) Supervisor I to join the Validation team. You’ll supervise a small team carrying out CSV activities across facilities management software and equipment software.

You will monitor milestones, ensure documented evidence, and prepare and approve validation documents in line with GMP and SOPs. Strong communication and project-based experience are essential.