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Senior Quality Engineer

Austin Vita
Posted 5 hours ago, valid for 6 days
Location

Bedale, North Yorkshire DL8 2NH

Salary

£48,000 - £57,600 per annum

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Contract type

Full Time

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Sonic Summary

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  • A Senior Quality Engineer position is available at a Global Medical Device company in North Yorkshire, offering a competitive salary of £50,000 to £60,000 per year.
  • The role involves supporting the compliance team to maintain necessary certifications and conducting internal audits in accordance with ISO 13485 and other regulations.
  • Candidates must have experience in the Quality environment within the Medical Device Industry, with a preference for those at Lead Auditor level.
  • Key responsibilities include managing non-conformities, preparing trending analysis data, and assisting with Quality Management System documentation.
  • The ideal candidate should possess strong interpersonal skills, attention to detail, and a proactive approach to problem-solving.
This is a fantasy opportunity for a Senior Quality Engineer to join a Global Medical Device company based in North Yorkshire. You will be responsible for supporting the compliance team to ensure all required certification is maintained.

Main Tasks/Responsibilities:

  • Complete internal audits in compliance with ISO 13485, 21 CFR, MDD/MDR and UKCA regulations.
  • Responsible for the logging, investigating, and documenting of non-conformities, ensuring appropriate action is taken to correct the issue and prevent recurrence, these must be completed within appropriate timescales including:
  • Corrective and Preventative Action Reports (CAPA)
  • Non-Conformity Reports (NC)
  • Regulatory reporting
  • Prepare trending analysis data whilst escalating any trends to a CAPA. Assist with preparation for the Quality Review Meeting.
  • Assist in the implementation of compliant processes and QMS documentation across multiple sites.
  • Responsible for the review and implementation of third-party agreements.
  • Undertake any other duties as may be requested.

Knowledge and Qualifications:


Essential:

  • Experience of working in a Quality environment, within the Medical Device Industry.
  • Experience of auditing to ISO 13485, preferably at Lead Auditor level.
  • Experience of generating and completing CAPA/Complaints and Root Cause Analysis.

Desirable:

  • Experience/knowledge of auditing the MDR, 21 CFR and UKCA regulations.
  • Experience/knowledge of reporting incidents to competent authorities.
  • Experience in writing processes compliant with standards.
  • Experience of ISO 14001.

Skills/Competencies:

  • Excellent interpersonal skills, including the ability to work as part of a team and to work with people from across the whole company.
  • Good organisation and leadership skills and attention to detail.
  • Good written and verbal communication skills.
  • A can-do attitude with the ability to take initiative and work to deadlines across multiple simultaneous tasks and projects
  • Problem Solver


Austin Fraser is committed to being an equal opportunities employer, and encourages applications from candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity status.

Due to the volume of applications received, we are unable to provide individual feedback to unsuccessful applicants.

Check us out on our websiteandLinkedIn for more roles.

We respect your personal data and would never offer it to third parties! For more information on how we handle your data, feel free to check out the Austin Fraser Privacy Noticeor contact (url removed) Austin Fraser International Ltd is registered in England: (phone number removed) Austin Fraser International Ltd, 33 Soho Square, London, W1D 3QU


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