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 7/8 qualification in Computer Science, Quality, Engineering or related discipline and 1-2 years working in a similar role with GMP exposure.
Responsibilities/ Duties:
The successful candidate will be a vital member of the Validation team working large scale projects for a variety of global Medical Device and Pharmaceutical leaders.
In this role, you will have the opportunity to participate in all aspects of the Validation Life Cycle. You will ensure our software solutions are delivered to the highest quality standards by collaborating with the Software Development team members.
You will be responsible for the validation of software, equipment and automation in accordance with the latest GMP, GAMP and FDA regulations.
You will also be responsible for all validation and change control documentation.
The successful candidate must have
Including DC Pension, Illness Benefit, Death in Service, Profit Share Scheme, Flexible working options, Career prospects, Training and Development.