Job Description
Hertfordshire
Permanent
Competitive Salary and Benefits
My client an expanding company in the medical device industry are seeking a QA Engineer to complete activities to meet regulatory, quality and business requirements.
Key tasks
Responsible for aspects of quality assurance activities, including;
·Internal audit programmes
·Quality Management System maintenance & compliance
·Document control:
oto include SOPs, internal audit files and other controlled documents.
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.