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Quality Assurance Specialist – Cambridge

Newton Colmore Consulting Ltd

United Kingdom

On-site

GBP 60,000 - 80,000

Full time

2 days ago
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Job summary

Ein wachsendes Unternehmen im Bereich Medizinprodukte sucht einen Quality Assurance Specialist in Cambridge. Diese Rolle bietet die Möglichkeit, ein Qualitätsmanagementsystem nach ISO 13485 zu entwickeln und technische Unterlagen für verschiedene Produktlinien zu erstellen. Ideal für jemanden mit ein paar Jahren Erfahrung, der in die Medizinproduktebranche einsteigen möchte oder mehr Verantwortung übernehmen will. Die Position erfordert tägliche Anwesenheit im Büro, mit der Aussicht auf hybrides Arbeiten. Bewerben Sie sich jetzt, um diese spannende Gelegenheit nicht zu verpassen!

Qualifications

  • Erfahrung im Qualitätsmanagement oder Qualitätsingenieurwesen.
  • Verständnis von ISO 13485 Standards ist von Vorteil.

Responsibilities

  • Entwicklung und Verwaltung des QMS-Systems für ISO 13485 Standards.
  • Erstellung und Verwaltung technischer Unterlagen für medizinische Geräte.

Skills

Qualitätsmanagementsystem (QMS)
ISO 13485 Standards
Regulatory Affairs
Qualitätsprüfung

Education

Bachelor-Abschluss in einem relevanten Fach

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.

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