Quality Technician

SRG; Shotwick; On-site; GBP 25,000 - 35,000; Full time

Job summary

A global medical device manufacturer is seeking a QA Technician in Shotwick, UK, to ensure product quality and compliance with regulatory standards. You will conduct routine testing, inspections, and support continuous improvement. The ideal candidate has experience in quality assurance, strong knowledge of inspection techniques, and excellent attention to detail. This is a unique opportunity to work in a dynamic environment committed to improving patient outcomes.

Qualifications

• Previous experience in quality assurance within a regulated industry, ideally medical devices.
• Strong understanding of inspection techniques and statistical sampling is essential.
• Familiarity with NC and CAPA processes is a must.
• Excellent attention to detail and strong problem-solving skills required.
• Ability to work collaboratively in a fast-paced environment.

Responsibilities

• Perform statistical sampling and inspection activities across all production lines.
• Verify and approve initial and final production pieces for compliance.
• Support rework activities related to inspection and testing processes.
• Assist in NC and CAPA investigations to resolve quality issues.

Skills

Quality assurance experience

Inspection techniques

Statistical sampling

Attention to detail

Problem-solving skills

Job description

About Us

We are recruiting for a global medical device manufacturer committed to delivering high‑quality products that improve patient outcomes.

As a QA Technician

You will play a critical role in ensuring product quality and compliance with regulatory standards. You will perform routine testing and inspection activities across multiple production lines, supporting continuous improvement and maintaining the highest standards of safety and reliability.

Key Responsibilities

• Routine Testing & Inspection (60%): Perform statistical sampling and inspection activities across all production lines.
• First Piece / Last Piece Inspection & Approval (20%): Verify and approve initial and final production pieces to ensure compliance with specifications.
• Inspection/Test Related Rework (10%): Support rework activities related to inspection and testing processes.
• Support NC & CAPA Investigations (10%): Assist in Non‑Conformance (NC) and Corrective and Preventive Action (CAPA) investigations to resolve quality issues.

Qualifications & Skills

• Previous experience in quality assurance within a regulated industry (medical devices preferred).
• Strong understanding of inspection techniques and statistical sampling.
• Familiarity with NC and CAPA processes.
• Excellent attention to detail and problem‑solving skills.
• Ability to work collaboratively in a fast‑paced environment.Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy