Quality Product Associate – Medical Devices

The Opportunity

Medasil Surgical Limited are seeking a Product Quality Associate to join our Quality team. This role is ideal for candidates with 1 to 2 years’ experience in Quality Control, Quality Assurance, Medical Device Manufacturing, or extensive experience within Cleanroom production environments who are looking to develop a career in Quality.

This is an excellent opportunity for a quality-focused professional with experience in regulated manufacturing and cleanroom environments to play a key role in maintaining product compliance, supporting production quality, and driving continuous improvement initiatives.

You’ll be joining a collaborative Quality team where your work will directly contribute to product safety, operational excellence, and regulatory compliance.

This role is full time onsite in Leeds so is suitable only for candidates who are within a commutable distance or are actively looking to relocate to Leeds.

There is no visa sponsorship for this role so only apply if you have full right to work in the UK.

Medasil Surgical Limited, established in 1974, is a renowned manufacturer of silicone tubing and surgical devices utilized in operating theatres. Based in Leeds, the company supplies high-quality medical devices to the NHS, private hospitals, and specialist clinics across the UK, as well as exporting globally.

The successful candidate will be supporting manufacturing on a daily basis, contributing to quality activities, conducting inspections, overseeing cleanroom compliance, and ensuring products meet customer, quality, safety and regulatory standards and requirements.

• Performing incoming goods inspections and product release activities
• Conducting in-process quality inspections and final product sign-off
• Supporting all manufacturing functions with packaging compliance
• Coordinating environmental and bioburden monitoring for external contract service provider testing
• Assisting with CAPA investigations and continuous improvement activities
• Maintaining equipment calibration records and inspection logs
• Supporting operator training and compliance procedures
• Reviewing manufacturing processes and identifying improvement opportunities
• Ensuring compliance with ISO standards and medical device regulations
• Supporting documentation updates and quality records management

• 1–2 years’ experience in a Quality Control, Quality Assurance, or manufacturing role within medical devices, biotechnology, or another highly regulated industry
• OR substantial cleanroom manufacturing experience and a genuine interest in moving into Quality
• Understanding of cGMP, cleanroom disciplines within regulated manufacturing environments
• Strong attention to detail and excellent organisational skills
• Good written and verbal communication skills
• Experience using Microsoft Office applications, particularly Excel and Word
• A positive attitude and willingness to learn

• Experience with in a medical device manufacturing environment
• Knowledge of ISO 9001, ISO 13485, MDR/MDD regulations, and QMS systems
• Understanding of LEAN principles and continuous improvement
• Strong communication and organisational skills
• Ability to work to deadlines
• Awareness of the Health and Safety at Work Act 1974
• Experience using Share Point

Full right to work in the UK - no visa sponsorship available.