A rare opportunity to join this highly respected organisation as a Validation Engineer.
*Develop protocols and reports in line with corporate validation requirements.
*Working with engineering groups to establish process capability studies.
*The ongoing drive to improve overall site quality performance by use of root cause analysis tools and techniques, with a specific focus on process capability
*Experience of working within a regulated industry with knowledge of MDD (Medical Device Directive), ISO 13485 (Quality Management Systems), FDA, cGMP, and Risk Management (ISO 14971)
*Experience in a supervisory or leadership role with people management responsibility
*Ability to work with cross-functional teams, including production, quality, engineering and materials.
*Experience working with moulding and extrusion processes and with automated assembly processes is desirable.
*Ability to multi-task and to work in a highly organised and friendly environment with an awareness of continued impact on production.
*Relevant experience in Metrology is a distinct advantage.
*A minimum of 2 years’ experience working in the medical device industry with focus on validation activities and process capability
*Experience working with quality engineers or direct experience in a quality role with active involvement with the manufacturing floor.