Quality Assurance Engineer - Med Device

JR United Kingdom; Peterborough; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading medical device company in Peterborough is seeking a Quality Assurance Engineer to ensure product compliance and customer satisfaction. The ideal candidate will have a relevant degree and proven experience in Quality Systems, with practical knowledge of regulatory frameworks like ISO 13485. This role includes supporting audit preparations and day-to-day quality operations.

Qualifications

• Proven industry experience in Quality Systems implementation.
• Practical knowledge of ISO 13485, CAPA requirements, GDP, and GMP.

Responsibilities

• Support the development of the site Quality Management System.
• Conduct internal quality audits and prepare audit reports.
• Provide guidance on non-conformances and support manufacturing operations.

Skills

Quality Systems

Regulatory Compliance

Internal Audits

Supplier Quality

Education

Relevant degree in a scientific or engineering discipline

Job description

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Quality Assurance Engineer - Med Device, Peterborough

Client:

Hyper Recruitment Solutions

Location:

Peterborough, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

1

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

ROLE OVERVIEW

We are currently looking for a Quality Assurance Engineer to join a leading medical device company based in the SEERS Medical area. As the Quality Assurance Engineer, you will be responsible for ensuring that products and services are fit for purpose, legally compliant, and meet customer expectations.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Quality Assurance Engineer will include:

• Supporting the development of the site Quality Management System (QMS) to meet business requirements.
• Conducting internal quality audits and preparing audit reports.
• Supporting preparation for customer, regulatory, and notified body audits.
• Providing guidance on non-conformances and supporting day-to-day manufacturing operations.

ROLE REQUIREMENTS:

To be successful, candidates should have:

• A relevant degree in a scientific or engineering discipline.
• Proven industry experience in Quality Systems and their operational implementation.
• Practical knowledge of ISO 13485, CAPA requirements, GDP, and GMP.

Keywords: Quality Assurance Engineer, Quality Systems, ISO 13485, CAPA, GDP, GMP, Quality Management System, Medical Devices, Regulatory Compliance, Internal Audits, Supplier Quality

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.