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Production Quality Engineer - Medical Devices
Newton Colmore Consulting Ltd
West Devon
On-site
GBP 40,000 - 45,000
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Job summary
Ein innovatives Unternehmen im Bereich Medizintechnik sucht einen erfahrenen Qualitätsingenieur, der eng mit dem Produktionsteam zusammenarbeitet. In dieser Schlüsselrolle sind Sie dafür verantwortlich, dass die gelieferten Teile den Designvorgaben und Qualitätsanforderungen entsprechen. Ihre Aufgaben umfassen die Durchführung von Qualitätsbewertungen bei Lieferanten, die Pflege der Device History Records und die Sicherstellung der Einhaltung von Dokumentations- und Beschwerdeprozessen. Das Unternehmen bietet nicht nur ein wettbewerbsfähiges Gehalt, sondern auch hervorragende Karrierechancen und praxisnahe Schulungen. Wenn Sie eine Leidenschaft für Qualität in der Medizintechnik haben, könnte dies die perfekte Gelegenheit für Sie sein.
Qualifications
- Erfahrung in der Qualitätskontrolle von Medizintechnikprodukten.
- Starke Kenntnisse in Dokumentenmanagement und Inspektionstests.
Responsibilities
- Überwachung der Qualität von Lieferanten und Sicherstellung der Einhaltung von Spezifikationen.
- Durchführung von Eingangskontrollen und Bearbeitung von Kundenrücksendungen.
Skills
Qualitätskontrolle
Dokumentenmanagement
Inspektionstests
Medizintechnologie
Education
Bachelor in Ingenieurwesen oder verwandtem Bereich
Tools
ISO 13485
QMS
ISO 14971
Job description
Salary: GBP40000 - GBP45000 per annum + Negotiable
Newton Colmore is working with a medical technology company near Lichfield, and we are assisting them with their search for a key quality hire to work closely with their production team.
The role as an experienced quality engineer will give you the opportunity to work on market leading medical devices whilst working closely with the production team to ensure that the parts delivered from the company’s suppliers meet the design specifications and quality requirements. The quality engineer will help the production team in supplier quality assessments including creating and following up on SCARs and will also ensure that the Device History Record (DHR) is up to date for products manufactured. This is a key new role within the team, and you will be reporting directly to the head of the team and collaborating with the five members of the production team.
This role will also cover key responsibilities such as incoming inspection of parts, customer returns, and ensuring that document control, CAPA, and the complaints process is followed effectively.
The company is looking for an experienced quality engineer with medical technology knowledge, mixed with strong document control and inspection testing skills.
In return for your hard work the company offers a competitive salary and benefits package as well as providing excellent career progression opportunities and hands-on training.
In regard to the process, there is a two-stage interview process where you will be invited to showcase your skills and experience, while finding out more about the company, their mission, and what they can offer you.
To enter the recruitment process click apply now and if you have the right skills and expertise, I will be in touch to discuss the opportunity further.
Keywords: Medical Devices, Quality Engineer, Quality Control, ISO 13485, QMS, Project Engineer, ISO 14971
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