Description
Senior Validation Engineers required for long term contract opportunities working with a market leading Medical Device manufacturing organisation located in Ireland. Due to site expansion and improvement projects our client is looking for 3 Senior Validation Engineer`s to support the activities of Operations and Engineering in assuring compliance with all relevant regulations.As the Validation Specialist you will be working with all departments ensuring operational effectiveness and developing product Quality for business continuity and process / product introductions.
Responsibilities:
* Develop Validation Documentation to support new process/product introductions and existing business continuity and process improvement requirements.
* Implement relevant policies and procedures.
* Work with the various departments / groups in development and execution of validation activities associated with new equipment / product or IM System upgrades.
* Run / Manage complaint investigation and resolution of same.
* Design and develop validation documentation to support business continuity, new process introductions...
* Implementation and co-ordination of the change control process, promotes timely approval of all supporting documentation.
* All employees are responsible for minimising both the Environmental and Health & Safety effects of the work that they perform.
Skills/Experience required:
* Degree qualified in a relevant subject
* Experience working within a Medical Device/Biotech/Pharmaceutical manufacturing environment
* Full validation life cycle experience is required