Job Description
Hertfordshire
Permanent
Competitive Salary and Benefits
My client an expanding company in the medical device industry are seeking a Quality Engineer
to carry out activities to meet regulatory, quality and business requirements.
Key tasks
·Maintain Internal audit programme.
·Quality Management System maintenance
·Document control lead for external audits.
·Construct/maintain documents to include SOPs, internal audit files and other controlled documents.
·Ensure Quality Management System compliance.
Essential Requirements
·Degree qualified or equivalent.
·Worked in medical device industry for minimum of 3 years.
·Worked in a regulated environment in line with ISO 13485 and US FDA 21 CFR 820.
·Certified Quality management systems auditor
·Proactive and self-motivated.
·Strong ability to multi-task.
If this role is of interest please apply with your most recent CV or contact Harrison Smith at Entech Technical Solutions Limited.