As a leading specialist recruiter and preferred supplier to the Medical Device and Technology sectors we have a continuous flow and good selection of Quality Auditor opportunities throughout the UK.
So if you are looking for career progression, a new challenge or a change of environment we are confident we can provide a short-list of exciting opportunities.
You can find a list of our latest Quality Auditor Jobs below!
For a confidential discussion to plan your next career move please contact our specialist Medical Device Consultant on +44 (0)121 616 3460 or ‘Register Your CV’ using the menu option on the left!
Clearly demonstrate good working knowledge of ISO 13485 and ISO60601 Medical Device Directive, experience in meeting regulatory requirements (CE Marking, FDA) and obtaining FDA 510K. You will be providing strong regulatory support within the offices being the main point of contact to see to issues raised by the worldwide offices along with client issues and certification.
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Clearly demonstrate good working knowledge of ISO 13485 and ISO Medical Device Directive, experience in meeting regulatory requirements (CE Marking, FDA) and obtaining FDA 510K. You will be providing strong regulatory support within the offices being the main point of contact to see to issues raised by the worldwide offices along with client issues and certification.
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Your key responsibilities will include managing the internal auditing program, providing reports to the quality systems review meeting to maintain lead auditor training. You will also be closely working alongside QA/RA and manufacturing engineers to ensure that all requirements have been adhered to, you will also be responsible for documentation completion and understand protocols and reports.
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This role will be office based however they will considered home based after initial training is completed. The job role will involve some world travel to complete on site audits. You will be working alongside an extremely highly regulated team performing key responsibilities; to assist in the management the global procedural documents quality management systems for Medical Devices, assist in the preparation and maintenance of a global audit schedule for Medical Device need to clearly demonstrate good working knowledge of ISO 13485 and Quality Management, experience in meeting regulatory requirements . Conduct technical filing, along with planning and managing the key assessment set.
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Your key responsibilities will include managing the internal auditing program, providing reports to the quality systems review meeting to maintain lead auditor training. You will also be closely working alongside QA/RA and manufacturing engineers to ensure that all requirements have been adhered to, you will also be responsible for documentation completion and understand protocols and reports.
ApplyView Detail
Quality Assurance Engineer – Medical Devices – Oxford
A fantastic opportunity has arisen for a Quality Assurance Engineer to join a leading worldwide Medical Devices company that specialise in providing highly dedicated solutions in the healthcare delivery and many more other worldwide solutions.
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Quality Assurance Engineer – Medical Devices – Oxford
A fantastic opportunity has arisen for a Quality Assurance Engineer to join a leading worldwide Medical Devices company that specialise in providing highly dedicated solutions in the healthcare delivery and many more other worldwide solutions.
ApplyView Detail