Due to large scale Biotech project wins we now wish to a Lead CQV Document Preparation Engineer to join our highly skilled PM Group team based onsite with a Biopharma client site in Carlow. Initially the successful incumbent can be Cork based (if prefered) but as the project continues a presence in Carlow would be required.
This role requires an individual who enjoys working with documentation ensuring accuracy, that all technical data required is included in the CQV documents and timely delivery of the documentation at each stage of the project.
We are looking for engineers with previous experience in the following areas:-
Third level Degree in relevant discipline
Minimum of 8 years engineering experience in a mechanical / process type background is essential
Some form of compliance type experience is desirable
This is an immediate requirement.
All CV’s are treated in the strictest confidence.
Recruitment agencies need not apply.
Do you have what it takes ?
Cork or Carlow, Ireland