Pharmaceutical Site Equipment Engineer Role
We are seeking a highly skilled engineer to coordinate and direct site equipment, utilities, processes, and software validation at a state-of-the-art pharmaceutical facility in Ireland.
Key responsibilities include:
* Equipment Validation Management: Generation and execution of Site Validation Master Plans and Project Validation Plans.
* Validation Protocol Development: Development and execution of validation protocols and final reports.
Candidates must possess a qualification or degree in engineering or a scientific discipline, along with 3+ years of validation/Quality experience in medical device plastics processing, moulding, or assembly operations. Knowledge of cGMP and regulatory requirements for the medical device industry is also essential.
This is a 12-month contract position located in Sligo, Ireland. The successful candidate will have excellent communication skills and the ability to work independently.