A new role has just been released by our partnered key client and we invite applications for the role of Quality Specialist from candidates with experience gained within the Regulatory Medical Device arena.

To be considered for this key appointment, which will enhance the existing quality team, you should ideally be Degree educated in a relevant scientific discipline and hold strong knowledge of relevant QMS systems and standards/regulations such as ISO 13485.

This knowledge and practical skill will allow you to support the Quality Manager and wider business to ensure its product registrations and technical documentation is controlled and compliant. Managing the product and service standards alike to meet the agreed protocols and record all activity in line with the business objectives.

You will be able to demonstrate your ability to meet the requirements above and also hold a strong communication style, both verbal and written in all formats. Your strong attention to detail, methodical work ethic and report writing skills will also be evident in your prior experience.

If you feel you can meet the requirements for this role please apply with an up to date CV today and indication of your salary expectation. The successful person will achieve a competitive local salary and a range of benefits on joining this growing, well positioned business.



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