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Senior Quality Engineer

Date: 06-Jul-2019

Location: Bishops Stortford, HRT, GB, CM23 3LJ

Company: Steris Corporation

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

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Are you experienced in combined Manufacturing and Quality Engineering/Quality Systems within the medical device industry?

Do you have experience with statistical analysis software and Visio?

If so, Steris are looking for a Senior Quality Engineer to support the continuous development, maintenance and improvement of STERIS quality systems. If you have excellent statistical analysis and problem-solving skills, and the ability to work collaboratively with cross-functional teams then we would love to hear from you. If this Senior Quality Engineer position sounds like an exciting opportunity for you, please apply today!

Position Summary

As Senior Quality Engineer, you will be responsible for planning and executing activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems.

With the use of statistical techniques and other quality principles, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement. 

Duties

With the use of statistical techniques and other quality principles, you will support complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement. 

Other duties will include:

  • Participate in cross-functional new product development teams with focus on the execution of quality plans and design transfer
  • Develop and implement statistically valid sampling plans, designed experiments, capability studies, SPC and trend analysis
  • Lead and/or participate in process/product corrective actions and problem-solving activities
  • Continuously review systems and perform statistical analysis, making recommendations to improve systems and the quality of process and product
  • Lead projects focused on system, product and service quality improvement 
  • Report on the performance of the quality system. 
  • Participate in and support strategic planning and audits
  • Supervision of Quality Engineers and other Quality staff

Required Experience

Key Skills, Responsibilities and Attitudes

  • Experience of combined Manufacturing/Quality Engineering and/or Quality Systems experience, working in an ISO certified environment preferably with medical device or other regulated industries

  • ASQ, QSR or familiarity with QSR/GMP regulations preferred

  • Experience with statistical analysis software and Visio preferred

  • Excellent problem-solving, organisational and communication skills

  • Focus on identification of potential issues and continuous improvement

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STERIS plc is a $2B+, publicly traded (NYSE: STE) organization with more than 12,000 employees worldwide.

STERIS strives to be an Equal Opportunity Employer.