Job Overview
We are seeking a skilled Validation Specialist to support our validation activities and ensure the quality of new tools and product introductions.
* The successful candidate will be responsible for writing and executing process validation protocols and reports for new product introductions and revalidations.
* They will develop and implement solutions to sustain and improve our Quality Management System (QMS).
* Maintenance of compliance to ISO 13485 and ISO 14001 systems standards is also an essential requirement.
Requirements:
A third-level qualification in Engineering, Polymer Science, or equivalent is required.
Minimum 5 years experience working with Medical Devices and strong expertise in Injection Moulding and Lean Six Sigma methodologies are necessary.