Quality Engineer - new job in Renfrewshire, UK

Quality Engineer
  • £30,000 - £33,000 per Annum
    ANNUM
  • Permanent
  • Renfrewshire, Scotland, UK Renfrewshire Renfrewshire UK PA4 9RR
Job Ref: J2165971
Sector: Engineering
Sub-sectors: Biotech/Life Sciences, Medical Devices
Date Added: 19 July 2022
Quality Engineer (Supplier, Risk, CAPA, Design) roles available for a thriving, established medical technology company based in Renfrew.

Here at SRG, we partner with a global medical device company dedicated to developing solutions for aortic and peripheral vascular disease. They are seeing great growth now and are seeking to grow their quality team. The roles they have available are:

  • Quality Engineer Process x 2
  • Quality Engineer Design
  • Quality Engineer CAPA x 2
  • Quality Engineer Risk

We are looking for people to apply for this role who have experience with some of the following:

  • Relevant science or engineering degree desirable
  • Six Sigma qualified - minimally Green Belt level desirable
  • Knowledge and understanding of applicable regulations especially with regards to Complaints, NCR/ CAPA processes and Root Cause Analysis/Trend Analysis
  • Class Ill medical device knowledge (desirable)
  • Proven experience of working in a global company within a regulated industry, preferably medical device or pharmaceutical manufacturing
  • Working knowledge of Minitab/Power Bi or similar statistical tools
  • Experience of FDA regulations
  • Thorough knowledge of regulatory standards, Quality Management Systems and global regulations for medical devices
  • Qualification or training experience in risk management, risk assessments or other comparable activity
  • Extensive and proven experience in Quality Systems in a similar role within a medical device environment
  • Solid experience in a global company within a regulated industry, preferably medical device or pharmaceutical manufacturing
  • Experience of Medical Device Directive and related regulations, preferably for Class Ill devices
  • Thorough knowledge of regulatory standards, Quality Management Systems and global regulations for medical devices
  • Knowledge and understanding of applicable regulations especially with regards to Complaints, NCR/ CAPA processes and Root Cause Analysis/Trend Analysis
  • Class Ill medical device knowledge (desirable)
  • Proven experience of working in a global company within a regulated industry, preferably medical device or pharmaceutical manufacturing
  • Working knowledge of Minitab/Power Bi or similar statistical tools

SRGTalent https://www.srgtalent.com https://www.srgtalent.com/-/media/srg/1---new-website/logos/website-logo-all-padding-removed.png
18/08/2022 16:19:11
GBP 30000 33000 Annum

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