Manager/Quality Manager

3 weeks ago

Cambridgeshire, United Kingdom Vector Recruitment Ltd Full time €50,000 - €75,000

Quality Manager Cambridgeshire
£50k-£75k (dep on exp) + bonus & excellent benefits

A fantastic opportunity for a Quality Manager has arisen at a Cambridge based cutting edge leading product development company whose innovative technology is reshaping the medical, life science and research sectors

The Quality Manager will be an integral member of the company’s management team focused on the development and implementation of quality procedures and processes at this fast growing and successful complex small electro-mechanical instrumentation manufacturing business.

As the Quality Manager, you will be responsible for managing all aspects of the quality department and it’s QMS whilst implementing and improving processes across all departments – from goods in, through production, quality control through to product delivery
You will take responsibility for all quality-based documentation and standard operating procedures (SOPs) not to mention related audits (both internally and externally) to ensure all parties are at the appropriate standard (ISO 13485) - working with internal stakeholders, customers and suppliers to ensure the delivery of high product quality across the business.

You will be a leading driver of quality processes throughout the company – putting your stamp on how all processes are done to the highest standards whilst fostering a continuous improvement mentality.
This is an all-encompassing role where you will utilise all your skills and experience of both technical and commercial nature – being the quality authority on site

The Quality Manager will need the following skills and experience:

Strong academic background - A Bachelor’s or Master’s degree in a relevant technical discipline
Practical, hands-on approach to quality processes in manufacturing and service provision
Recent and relevant experience in a senior quality role (e.g. Quality Manager / Deputy Quality Manager / Senior Quality Engineer) within a medical device manufacturing environment
Extensive experience within Quality Management Systems along with the medical device standards of ISO 13485.
Advanced Quality knowledge (e.g. PPAP, FMEA], CAPA, continuous improvement, problem solving, 5S, Risk Assessment, etc.)
Excellent attention to detail goes without saying, thus experience of technical writing and drafting formal quality documentation would be required.
Experience managing customer audits, and conducting supplier audits (both onsite and remote)

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