Biovalidation Engineer Role
We are seeking a highly experienced Biovalidation Engineer to fill this key position at our state-of-the-art manufacturing facility in Dublin.
The ideal candidate will have extensive knowledge and demonstrated experience executing validation activities for pharmaceutical projects, with a strong understanding of safety and GMP requirements.
Key Responsibilities:
* Execute validation activities associated with a Sterile Fill Finish process
* Develop and implement CQV test documentation
* Contribute to site validation master plans and standard operating procedures
* Analyze and report on relevant validation data/metrics
* Assist in exceptions and deviation resolution and root cause analysis
Requirements:
* 6+ years experience in Engineering or Validation
* Technical qualification at third level or equivalent in Engineering
* Extensive knowledge and demonstrated experience executing validation activities for Pharmaceutical projects
* Experience of sterile equipment within the pharmaceutical industry is preferred
About this role:
This is an exciting opportunity to join our team and take your career to the next level. If you are looking for a challenging and rewarding role, we encourage you to apply.