Are you an experienced Quality Manager seeking a new role? Would you like to work for a global company who offer 25 days annual leave plus bank holidays? Free parking and incredible benefits including up to 8% employer pension contribution, a staff barbecue in the summer and team nights out? Working Monday - Friday 9am-5pm NO SHIFTS! If the answer is yes then read on about this incredible opportunity.

As the Quality Manager you will be responsible for:

* Responsible and accountable for all aspects of Quality at our clients site
* Develop annual Quality strategy aligned to a site strategy, KPIs and organisational goals to transition from QC to QA Monitor, review and maintain the ISO 9001 and ISO 13485 requirements at our clients site
* Maintain all documentation within the Quality area, and responsible for monitoring control of documentation throughout all areas.
* Provide leadership, direction and development to Quality Team employees whilst developing a high performing team, maintaining agreed standards individually and corporately, taking necessary action to address performance levels including annual appraisals.
* Develop and maintain a collaborative and supportive relationship with all other departments at site and in the wider organisation/matrix
* Generate and implement ideas that improve quality indicators, in line with cost, investment and service goals. Implement Lean Tools and practices - TQM, PPM, SPC.
* Lead the Non conformance and CAPA process to ensure true root cause is identified and remediated in a timely manner.
* Ensure a robust change management process is maintained across the site.
* Maintain and enhance the site Validation Master Plan, and develop and update new validation protocols
* Generate reports of non-conforming product internally and externally against individual departments
* Maintain close contact with technical services and/or customers concerning quality related concerns, requests and/or issues
* Actively involved in R & D for new / existing tooling and implementation of customer requirements
* Provides technical guidance and works closely with R & D, Product management, Manufacturing and Distribution on major new product introductions and acquisitions
* Assist R & D functions in planning of new tooling and associated test jigs/equipment
* Participate in divisional QMS projects incl. implementation of electronic QMS at Ashford Site



Our client would like to recruit someone with:

* Experience in a Quality environment within forensic or laboratory products
* Solid background from ISO 9001:2008 and some experience with ISO 13485:2003 experience
* Working knowledge of ISO9001:2015 and ISO13485:2016 to be preferred
* Proven ability to standardise, implement and improve processes
* Strong capabilities within Root Cause Analysis
* Degree educated preferably within a Scientific discipline
* Lead Auditor Qualification & experience of internal, external and supplier auditing

This role is working Monday - Friday 9am-5pm. Our client can interview immediately and is looking forward to someone joining their incredible organisation.

We look forward to your application.

Office Angels is an Equal Opportunities Employer, and works as a Recruitment Agency for Permanent vacancies. Please be aware that we are currently receiving a high volume of applications and will endeavour to contact all applicants, however if you have not been contacted within 72hrs please assume that you have not been successful on this occasion and your CV will be kept on record for future positions.

Office Angels is acting as an Employment Agency in relation to this vacancy. The Adecco Group UK & Ireland is an Equal Opportunities Employer.