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SENIOR QUALITY ASSOCIATE /QUALITY ENGINEER

Job Title: SENIOR QUALITY ASSOCIATE /QUALITY ENGINEER
Contract Type: Permanent
Location: Leeds, West Yorkshire
Industry:
Salary: £28000 - £34000 per annum + Benefits
Start Date: ASAP
Reference: J895899_1531479536
Contact Name: Ben George
Contact Email: ben.george@russell-taylor.co.uk
Job Published: July 13, 2018 11:58

Job Description

Role: Senior Quality Associate / Quality Engineer

Location: Leeds

Salary: Competitive

Russell Taylor Group has a fantastic opportunity for a Quality Associate / Quality Engineer that specialises within ISO 13485 Medical Device Industry. You will have experience working within a Quality Team, be an excellent team player and have excellent attention to detail. If you're looking for a new company that offers excellent work / life balance and new challenge please do not hesitate to apply within.

Role:

  • Conduct CAPA investigations and identify appropriate corrective actions with a specific focus on engineering issues.
  • Facilitating problem solving and root cause analysis for quality issues using tools such as 8D Problem Solving
  • Identify appropriate technical colleagues to take part in review groups and chair groups in relation to investigations.

  • Conduct investigations into complaints with a specific focus on engineering issues and write reports and recommendations. Liaise with complainants as required.
  • Data collection, analysis and trending with the aim of reducing non- conformities and raising any Corrective Action or preventative action reports required.
  • Reviewing inspection data and trends established by Quality Control and working with Quality Control and Manufacturing with a view to identifying root cause of issues and determining improvements.
  • Undertake any other duties as may be requested by the Quality Systems Manager or Compliance Director.

Person:

  • Degree in engineering.
  • Experience of working in a Quality environment, preferably within the medical device industry, but other related industries would be considered.
  • Experience of CAPA and root cause analysis.
  • Working to a recognised QMS; preferably ISO 13485, but those with experience of ISO 9001 will also be considered.

Keywords: Quality Associate, Quality Engineer, 13485, CAPA, QMS, Medical Device,

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