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Quality Assurance Engineer - Med Device

JR United Kingdom

Crawley

On-site

GBP 30,000 - 45,000

Full time

4 days ago
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Job summary

A leading medical device company in Crawley is seeking a Quality Assurance Engineer. The role involves ensuring product compliance with quality standards, conducting internal audits, and supporting the development of the Quality Management System. Candidates should possess a relevant scientific or engineering degree and experience with ISO standards.

Qualifications

  • Proven experience in Quality Systems and their operational implementation.
  • Practical knowledge of ISO 13485, CAPA, GDP, and GMP standards.

Responsibilities

  • Support the development of the site Quality Management System (QMS).
  • Conduct internal quality audits and prepare audit reports.
  • Assist in preparation for customer and regulatory audits.

Skills

Quality Systems
ISO 13485
GMP
CAPA
Regulatory Compliance

Education

Relevant degree in a scientific or engineering discipline

Job description

Quality Assurance Engineer - Med Device, Crawley, West Sussex
Client:

Hyper Recruitment Solutions

Location:

Crawley, West Sussex, 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 seeking a Quality Assurance Engineer to join a leading medical device company based in the SEERS Medical area. The successful candidate will ensure that products and services are fit for purpose, legally compliant, and meet customer expectations.

Key Duties and Responsibilities:
  1. Support the development of the site Quality Management System (QMS) to meet business requirements.
  2. Conduct internal quality audits and prepare audit reports.
  3. Assist in preparation for customer, regulatory, and notified body audits.
  4. Provide guidance on non-conformances and support manufacturing operations.
Role Requirements:

To succeed in this role, candidates should have:

  1. A relevant degree in a scientific or engineering discipline.
  2. Proven experience in Quality Systems and their operational implementation.
  3. Practical knowledge of ISO 13485, CAPA, GDP, and GMP standards.
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 all qualified individuals. HRS specializes in the Life Science sectors, combining recruitment expertise with scientific knowledge to support your career development.

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