Quality Engineer - Life Sciences | Lean, CAPA & RCA

QCS Staffing Ltd; Chester; On-site; GBP 42,000 - 52,000; Full time

Job summary

QCS Staffing is seeking a Quality Engineer for a UK Chester-based initial 6-18 month contract in Life Sciences. The role focuses on driving continuous improvement in quality, leveraging Lean, Six Sigma, and quality tools to enhance product quality and operational efficiency.

You will analyse quality metrics, identify improvement opportunities, and implement sustainable corrective actions. Cross-functional RCA facilitation will be key to reducing defects and improving process capability while

Qualifications

• Extensive experience in a quality engineering role, preferably in medical devices.
• Understanding of medical device regulatory requirements.
• Experience with CAPA and NC processes.
• Basic familiarity with eQMS or similar systems.

Responsibilities

• Drive continuous improvement using Lean, Six Sigma, and quality tools to improve product quality and process efficiency.
• Analyse quality metrics and trends to identify improvement opportunities and implement corrective actions.
• Facilitate cross-functional problem solving, including Root Cause Analysis (RCA), to reduce defects and improve process capability.
• Support risk reduction, cost reduction, and process optimization while ensuring regulatory compliance.

Tools

eQMS

Job description

Quality Engineer – Wales, Wrexham – Initial 6-Month Contract – Life Sciences

Our client is a global medical products and technologies company focused on solutions for the management of chronic conditions, with leading market positions in advanced wound care, ostomy care, continence care and infusion care.

Their products provide a range of clinical and economic benefits including infection prevention, protection of at-risk skin, improved patient outcomes and reduced total cost of care.

What You’ll Deliver

• Maintain and improve the Quality Management System in accordance with all applicable regulatory requirements
• Support process validation activities (IQ/OQ/PQ).
• Investigate product and process nonconformities.
• Manage and monitor Corrective and Preventive Actions (CAPA).
  
  

Key requirements include:

• Strong experience in a similar role, within Pharma, Biotec, or Medical Devices
• Basic knowledge and experience of CAPA and NC.
  
  

If this role is of interest, please apply now!