Quality Engineer, Medical Devices – QMS & CAPA Expert

BMS Performance Ltd

Wembley

On-site

GBP 50,000 - 55,000

Full time

14 hours ago
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Benefits offered by this job

25 days holiday + bank holidays
Learning & Development opportunities
Employee Assistance Programme
Online GP through Livi
Lifestyle discounts and team-building

Job summary

BMS Performance Ltd is seeking a Quality Engineer for our client in Wembley, a medical products business focused on advanced wound care and infection prevention. The role centers on maintaining the QMS, ensuring compliance with ISO 13485 and related standards, and driving continuous quality improvements.

You will support investigations, CAPA, supplier management, and product release, in a collaborative office setting at the Northwest London head office, requiring five days per week in the

Qualifications

  • Minimum 2 years' quality experience in medical device manufacturing.
  • Experience in ISO 13485 QMS.
  • Strong understanding of CAPA, change control, document control, and risk management.
  • Experience with supplier/subcontractor quality management and quality documentation reviews.
  • Knowledge of medical device regulations and international standards.

Responsibilities

  • Support and maintain the effectiveness of the QMS.
  • Ensure compliance with regulations and standards.
  • Support investigations, audits, CAPA, and supplier management.
  • Manage product release and ongoing quality improvements.
  • Role based at head office in Northwest London with five days in the office.

Skills

ISO 13485
CAPA
Document Control
Change Control
Risk Management
Internal Audits
Product Release
Supplier Quality
Regulatory Knowledge

Job description

BMS Performance Ltd is seeking a Quality Engineer for our client in Wembley, a medical products business focused on advanced wound care and infection prevention. The role centers on maintaining the QMS, ensuring compliance with ISO 13485 and related standards, and driving continuous quality improvements.

You will support investigations, CAPA, supplier management, and product release, in a collaborative office setting at the Northwest London head office, requiring five days per week in the

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