Quality Engineer

BMS Performance Ltd.; Greater London; On-site; GBP 40,000 - 50,000; Full time

Benefits offered by this job

25 days holiday + bank holidays

Learning & Development and career prog

Employee Assistance Programme and Well

Online GP through Livi

Lifestyle discounts and team-building

Job summary

BMS Performance Ltd. in Northwest London is seeking a Quality Engineer with at least 2 years' experience in medical device manufacturing to strengthen the QMS and ensure regulatory compliance. The role requires 5 days per week in the office at the head office.

You will lead CAPA, change control, risk management and supplier quality, support investigations and audits, and drive ongoing quality improvements within a regulated environment.

Qualifications

• Minimum 2 years' quality experience in medical device manufacturing.
• Practical experience with ISO 13485 / medical device QMS.
• Strong knowledge of CAPA, document control, change control and risk management.
• Familiar with supplier quality management and product release processes.
• Understanding of applicable medical device regulations and standards.

Responsibilities

• Support and maintain the QMS for regulatory compliance.
• Lead investigations, CAPA and change control activities.
• Perform internal audits and supplier management.
• Assist with product release and quality improvements.

Skills

Quality experience in medical device

CAPA

Document control

Change control

Risk management

Internal audits

Job description

Home Live Jobs Engineering Jobs Quality Engineer

• Join an established and growing medical products business operating within the advanced wound care and infection prevention sector.
• Work in a friendly, collaborative office environment where your voice is heard, your ideas are valued and you can work closely with colleagues across the business.
• A hands-on opportunity to make a genuine impact on quality, compliance and continuous improvement within a regulated medical device environment.

About the company

An established medical products manufacturer specialising in advanced wound care and infection prevention, developing products designed to improve patient care and support healthcare professionals. The business has a strong focus on quality, innovation and continuous improvement.

About the role

We are looking for a Quality Engineer with at least 2 years' experience within medical device or medical product manufacturing. You will support and maintain the effectiveness of the QMS, ensuring compliance with relevant regulations and standards while supporting investigations, audits, CAPA, supplier management, product release and ongoing quality improvements.

The role is based at the company's head office in Northwest London and requires 5 days per week in the office.

Requirements

• Minimum 2 years' Quality experience within medical device or medical product manufacturing.
• Practical experience working within an ISO 13485 / medical device QMS.
• Strong knowledge of CAPA, Document Control, Change Control, Risk Management, Internal Audits and Product Release.
• Understanding of applicable medical device regulations and international standards.
• Experience with supplier/subcontractor quality management and reviewing quality documentation.

Package

• 25 days holiday + bank holidays
• Learning & Development and career progression opportunities
• Employee Assistance Programme and wellbeing support
• Online GP through Livi
• Lifestyle discounts and team-building events