Quality Assurance Manager

CompanySovrin Medical Plastics

LocationSlough, England, United Kingdom

Posted At3/11/2026

UK Visa Sponsorship Analytics

Occupation Type

Quality assurance and regulatory professionals

Occupation Code Skill LevelHigher Skilled

Sponsorship Salary Threshold

£48,200 (£24.72 per hour)

Occupation rate applies

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Description

Quality Manager

Sovrin Medical Plastics Ltd
Location: UK (on-site)
Contract: Full-time, Permanent

About Sovrin Medical Plastics

Sovrin Medical Plastics Ltd is a well-established UK manufacturer specialising in medical device moulding and cleanroom manufacturing. With a long-standing reputation for quality, compliance, and technical excellence, we support leading medical and healthcare customers with precision injection-moulded components and validated manufacturing processes.

Operating within a regulated ISO 13485 environment, quality is central to everything we do.

The Role

We are seeking an experienced Quality Manager to lead and continuously improve our Quality Management System and ensure full compliance with ISO 13485 and applicable regulatory requirements.

This is a hands-on leadership role, working closely with Operations, Engineering, and Customers to ensure robust processes, effective risk management, and audit readiness at all times.

Key Responsibilities

Own, maintain, and develop the ISO 13485 Quality Management System
Act as site lead for external audits (customers, notified bodies, regulators) and internal audits

Manage CAPA, deviations, non-conformances, and complaints through to effective closure

Ensure compliance with regulatory and customer requirements for medical device manufacture

Oversee document control, change control, and validation documentation

Lead quality input into new product introduction (NPI) and process changes

Manage supplier quality, including supplier approval and performance monitoring

Drive continuous improvement and quality culture across the business

Provide leadership and mentoring to quality team members as their line manager

Skills & Experience Required

Proven experience as a Quality Manager (or Senior Quality Engineer) in a manufacturing environment
Strong working knowledge of ISO 13485 (medical devices essential)
Experience within plastic injection moulding, cleanroom, or medical manufacturing highly desirable
Confident leading audits and interfacing with customers and external bodies
Practical experience of CAPA, risk management, and validation activities
Strong attention to detail with a pragmatic, solutions-focused mindset
Excellent communication skills at all levels

Strong IT skills for working in a data-driven environment (ERP experience desirable)

What We Offer

Key leadership role within a respected medical manufacturing business
Opportunity to shape and strengthen quality systems and culture
Stable, long-term position in a growing and technically capable organisation
Competitive salary, commensurate with experience