We are looking for a Validation Engineer to join our expanding team the role will be based in the South-east and will involve working in a GMP environment.
The successful candidate must have a Level 8 qualification in Computer Science, Quality, Engineering or related discipline.
Responsibilities/ Duties:
- Prepare software validation protocols and test scripts in accordance with procedures.
- Execute test scripts and capture test evidence
- Software/Equipment Validation – Responsible for writing validation protocols, including test scripts and reports.
- Technical Writing including user requirements, SOPs and other Technical documentation.
- Work with Quality department to ensure validations are in line with customer validation standards.
- Create documentation and reports across the entire validation life cycle
- Project Management
The chosen candidate must have
- Level 8 qualification in Engineering, Computer Science, Quality or Validation related discipline. (Essential)
- 3 – 5 years’ experience in a similar role.
- Be very meticulous and can work to project deadlines. Excellent communication skills, written and verbal English communication is essential.
- Knowledge and experience of Software Development and Validation Life Cycle.
- Experience of working in a GMP medical device/pharma or similar environment
- GAMP experience is a distinct advantage
Including DC Pension, Illness Benefit, Death in Service, Profit Share Scheme, Flexible working options, Career prospects, Training and Development.
