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Senior Quality Engineer - South Wales

WALKER COLE INTERNATIONAL LTD
Posted 18 hours ago, valid for 14 days
Location

Cardiff, South Glamorgan CF5 1DR, Wales

Salary

£24,000 - £28,800 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Walker Cole International is seeking a Senior Quality Engineer for a Medical Device company located in South Wales.
  • The role involves process ownership of design quality and risk management, along with approving change management activities.
  • Candidates should have a detailed understanding of the Medical Device manufacturing process and experience with ISO 13485, GDP, and GMP.
  • The position requires a minimum of 5 years of experience in a related field, and proficiency in engineering and quality practices is essential.
  • The salary for this position is competitive and commensurate with experience.

Walker Cole International is searching for an Senior Quality Engineer to join a Medical Device company based in South Wales. As the Senior Quality Engineer, you will be responsible for process ownership of design quality and risk management sitewide and will approve change management activities from a risk and validation perspective.

Key responsibilities of the Senior Quality Engineer include:

  • Mentor and oversee validation plans, protocols, reports, and requirement specifications
  • Work closely with R&D, clinical and operations, and other business functions to ensure quality performance of product and process
  • Support internal and external audit processes
  • Initiate and lead the development of PHAs, pFMEAs, and dFMEAs

A successful Senior Quality Engineer will demonstrate:

  • A detailed understanding of the Medical Device manufacturing process
  • Proficiency in ISO 13485, Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP)
  • A good understanding of engineering and quality practices and methods
  • Excellent communication skills and attention to detail

Training in Lean Six Sigma project management approach is a distinct advantage.

Senior Quality Engineer | Validation | Risk Management | Medical Device | MD | Good Manufacturing Practice | GMP | Good Distribution Practice | GDP | Lean Six Sigma | ISO 13485 | Problem Solving | PHAs | pFMEAs | dFMEAs | Design Quality | Preliminary Hazard Analysis | Process Failure Mode and Effective Analysis | Design Failure Mode and Effective Analysis|

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.