Validation Engineer required for medical device manufacturing facility in Longford.
Will support the successful qualification of new tools / product introduction on-site.
Permanent role with benefits.
If interested, do email an updated word copy of your CV Role *Write and execute process validation protocols and reports for new product introductions and revalidations due to process /material improvements utilizing scientific / technical knowledge. *Developing and implementing solutions to sustain and improve the QMS. *Maintain and support compliance to ISO 13485 and ISO 14001 systems standards...