Head of Quality and Regulatory (Medical Devices)
Michael Page
This role is vital for the start up business’s compliance as they move towards commercialisation of a new product. The main duties would be related to QMS compliance, training staff on Quality and Compliance, and developing Quality strategy and operations moving forward.
– Full QMS oversight
– Training of staff internally RE Quality and Regulatory Compliance
– Internal/External audits
– Collaborating with wider business and key stakeholders
A truly hands on role|Full Quality autonomy
– ISO 13485 Expert
– Ability to work on-site in Southampton
– Confidence to be fully responsinble for a Quality System
A start up Medical Device business, currently in design and development stage.
– Competitive Salary
– Exciting future prospects
– A chance to join an exciting start up
£60000 per year
Southampton
Wed, 06 Mar 2024 23:47:01 GMT
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