Quality Assurance Officer

Job description

Are you detail‑driven, proactive, and passionate about maintaining high-quality standards? We’re looking for a Quality Assurance Associate to join an exciting medical device organisation and play a key role in supporting our Quality Management System and ensuring compliance with regulatory and industry standards.

About the Role

As a Quality Assurance Associate, you will help maintain and continuously improve the Quality Management System, ensuring products, processes, and documentation meet required regulatory and quality expectations. This is a fantastic opportunity for someone who thrives in a structured environment and enjoys working cross‑functionally to uphold excellence.

Key Responsibilities

• Support the maintenance and ongoing improvement of the Quality Management System in line with relevant regulations and standards (e.g., ISO 13485).
• Assist with developing, reviewing, and updating quality manuals, SOPs, and related documentation.
• Review and receipt Goods Received Notes (GRNs) for inbound containers, ensuring accuracy against supplier and shipment documentation.
• Evaluate pre‑production samples to verify compliance with approved specifications before full production.
• Support preparation for and participation in notified body audits.
• Monitor regulatory updates and help implement required changes.
• Liaise with suppliers and support supplier audits, including preparing approved supplier submissions.
• Assist with Corrective and Preventive Actions (CAPA).
• Manage and monitor product complaints.
• Support maintenance of MHRA registration.
• Review product labelling, packaging, and artwork for regulatory and procedural compliance.
• Maintain version control and ensure latest approved artwork/labels are used in production.
• Assist with change control activities related to product and process updates.
• Support employee training on quality procedures and requirements.

What We’re Looking For

• Strong attention to detail and organisational skills
• Ability to work independently and collaboratively
• Familiarity with quality standards (ISO 13485 preferred)
• Effective communication skills
• Previous experience in quality, regulatory, or a related field is a plus

Please note this role does not offer job sponsorship, and you must be able to work in the UK with no restrictions.

For more information please get in touch - jamie.keith@cpl.com

Extra information

Status

Open

Education Level

Secondary School

Location

Watford

Type of Contract

Full Time Jobs

Published at

09-03-2026

Full UK/EU driving license preferred

No

Car Preferred

No

Must be eligible to work in the EU

No

Cover Letter Required

No

Languages

English