On-Site Graduate Production Quality Engineer

KaneHR

Birmingham

Sur place

GBP 28 000 - 36 000

Plein temps

14 jours+

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Résumé du poste

Xstrahl is seeking a Graduate Production Quality Engineer for our Brownhills, UK site. You will develop build manuals, write work instructions, and perform system sign-offs on medical X-ray systems.

Expect to spend 1–2 days weekly on the production floor, capturing hand-on knowledge to document processes and support CAPA/NCR work. You will learn the manufacturing and qualification processes in a regulated medical device environment, with potential growth into broader manufacturing engineering

Qualifications

  • Degree in mechanical, electrical, electronic or related engineering.
  • Clear written communication to translate technical processes into instructions.
  • Organised with careful records and attention to detail.
  • Hands-on attitude and eagerness to learn how systems are built.
  • Willing to take ownership and complete tasks.
  • Proficiency with Microsoft Office.

Responsabilités

  • Build and maintain build manuals and work instructions for each system.
  • Test draft instructions on the production floor and update as needed.
  • Carry out system sign-off activities including electrical and mechanical checks.
  • Log, progress and close NCRs, CRs, PFRs and CAPAs.
  • Spend time on the production floor to build and understand each system.
  • Support process improvements and handover of new builds from R&D.

Connaissances

Clear writing
Attention to detail
Organised
Hands-on
Ownership
MS Office

Formation

Engineering degree

Outils

CAD software

Description du poste

Xstrahl is seeking a Graduate Production Quality Engineer for our Brownhills, UK site. You will develop build manuals, write work instructions, and perform system sign-offs on medical X-ray systems.

Expect to spend 1–2 days weekly on the production floor, capturing hand-on knowledge to document processes and support CAPA/NCR work. You will learn the manufacturing and qualification processes in a regulated medical device environment, with potential growth into broader manufacturing engineering

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