This is an excellent opportunity for an experienced QA professional from a Medical Device or IVD background. Supervisory experience is essential for this role.
The Ideal Candidate:
*Recent experience of working within a Medical Device or IVD Manufacturing Environment
*Supervisory/Line Management Experience
*Strong knowledge and proven experience of Production and Process Controls
*Qualified ISO 13485:2016 Auditor
Reference no: 7898
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