Quality Assurance Specialist - Cambridge

Newton Colmore Consulting Ltd; Cambridge; On-site; GBP 30,000 - 45,000; Full time

Job summary

A growing Medical Devices company in Cambridge is seeking a Quality Assurance Specialist to assist in developing their QMS system for ISO 13485 standards. This role offers a great opportunity for early-career professionals looking to take on more responsibilities and gain entry into the Medical Devices sector while operating with experienced mentors.

Qualifications

• Degree in a relevant field.
• Basic understanding of Regulatory Affairs is advantageous.
• Quality Assurance background preferred, experience in ISO standards helpful.

Responsibilities

• Assist in the development of QMS system for ISO 13485.
• Create and manage technical files for Medical Devices.
• Collaborate with manufacturing teams to ensure quality compliance.

Skills

Quality Assurance

Regulatory Affairs

ISO 13485

Quality Engineering

Education

Degree related to Quality Assurance or Quality Engineering

Job description

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Quality Assurance Specialist - Cambridge, Cambridge

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Client:

Newton Colmore Consulting Ltd

Location:

Cambridge, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

44675ad159b5

Job Views:

4

Posted:

25.06.2025

Expiry Date:

09.08.2025

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Job Description:

Quality Assurance Specialist - Cambridge

A growing Medical Devices company based in Cambridge is currently looking for a new Quality Assurance Specialist to assist in the development of the QMS system for ISO 13485 standards. They are open to candidates from alternative sectors, allowing for ISO 13485 standards training.

You will also be creating and managing technical files for several Medical Devices lines, including Class I, Class IIa and Class IIb Medical Devices. You'll collaborate with a number of Medical Devices experts, but you will be the sole person focusing on Quality Assurance duties. However, you will receive Quality Assurance assistance from the parent company's Quality Assurance Manager. Due to this, we are open to candidates who only have a couple of years of experience of ISO 9001 or QMS, but also keen to hear from people with more experience.

This is an excellent opportunity for someone a couple of years into their career and looking for more responsibility to lead the development of a QMS system, or for someone who is looking for a route into the Medical Devices sector under ISO 13485 standards. Due to the active work in setting up the QMS system, you will need to be in the office daily; however, over time there should be the opportunity for hybrid working.

It is expected that you would hold a degree in a subject that has led you into a Quality Assurance, Quality Engineering, or Design Assurance role.

Apart from having a Quality Assurance background, it would also be highly advantageous if you have a good understanding of Regulatory Affairs.

Part of your role will involve working alongside the manufacturing teams for these medical devices. Due to this, it would be highly beneficial if your Medical Devices Quality Assurance experience came from a Quality Engineering background, although this is not essential.

I anticipate a lot of interest in this role, so if you are interested, I suggest making an application now or risk missing out.

For more information, please feel free to call Andrew Welsh, Director of Medical Devices recruitment, Science recruitment and Biotech recruitment specialists Newton Colmore Consulting, on [phone] or make an application and one of our team at Newton Colmore Consulting will contact you.