Pro-Resourcing Ltd, are currently recruiting on behalf of our reputable client.

Our client, a well-established, globally recognised manufacturing business, currently requires a Quality Engineer to join their team.

The position is full time, permanent.

The Role

Determine the correct approach/next steps using risk based decision making. Author and review RCA (root cause analysis) and CAPA records. Lead process improvement activities. Design and set-up gauge R&R, equivalency and process capability studies. Present metrics and data on a routine basis to colleagues, peers and management. Interpret and ensure adherence to customer requirements. Author and approve QMS documentation. Ensuring processes needed for the QMS are established, implemented and maintained. Support NPI projects as required. Liaise with customers and be the point of escalation for any customer issues. Conduct 1:1 meetings with team members and perform other personnel meetings as required, e.g. probation reviews. Creating, completing and reviewing engineering change notes/change controls. Creating PFMEA s and conducting risk assessments. Liaising with all functions (including suppliers). Process evaluation and improvement fault root cause investigation and process controls implementation. Analyse data by completing hypothesis, normal distribution, and process capability analysis tests. Establishes statistical confidence by identifying sample size and acceptable error; determining levels of confidence. Prepares reports by collecting, analysing, and summarising data; making recommendations. Ensure that all products are thoroughly quality checked. Support and mentor Quality Controllers and Quality Inspectors. Develops sampling plans by applying attribute, variable, and sequential sampling methods. Responsible for training and development of Quality Controllers. Coordinate the implementation of new quality standards. Ensure that Client, Supplier and Internal Audits are carried out to the defined schedule.

Requirements

Quality management system principles and techniques. International & British Quality Standards (ISO 9001, ISO 13485, ISO 17025, ISO 14001, BS OHSAS 18001, FDA, QSR s and Medical Devices Directive). Quality toolbox including FMEA, Process flows, Root cause investigations, Lean and Six Sigma tools & techniques. Internal Audit experience to the relevant standards. Medical or Aerospace background would be beneficial. Experience working within a Quality process related role.

Working Hours: Monday to Thursday 08:30-17:00 (Including 1 hour break) and Friday 08:30-13:30 (35 hour working week)

Salary: GBP30,000 - GBP38,000 (Dependent on experience)

Benefits:

32 days holiday per annum including 8 statutory public holidays.

2 additional days holiday for ever 5 years in employment.

Company pension scheme.

Annual bonus if targets are met but not guaranteed.