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Quality Engineer

Meriden Media
Posted a day ago, valid for a month
Location

Nottingham, Nottinghamshire NG9 6HZ, England

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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  • The job is for a Quality Engineer with a salary of up to £42k depending on experience.
  • The position requires at least 5 years of experience in quality operations within biotech or pharmaceutical manufacturing.
  • The Quality Engineer will work closely with Operations, Manufacturing, R&D, and Quality teams to drive continuous improvement and ensure compliance with industry standards.
  • Key responsibilities include leading quality investigations, collaborating with cross-functional teams, and driving process improvement initiatives using methodologies like SPC, Six Sigma, and Lean.
  • Candidates must have a degree in Business, Sciences, or Engineering, along with strong knowledge of ISO 9001/13485 and regulatory compliance.

Quality Engineer Up to £42k DOEMonday - Thursday 07:00 - 16:00,Friday 07:00 - 13:00Seeking a Quality Engineer to work closely with Operations, Manufacturing, R&D, and Quality teams to drive continuous improvement and ensure compliance with industry standards. The role involves managing quality processes, investigating non-conformances, and implementing corrective and preventive actions (CAPA).Key Responsibilities:

  • Lead quality investigations for market defects, identifying root causes and implementing CAPA.
  • Collaborate with cross-functional teams on failure modes and impact assessments.
  • Interface with customers and suppliers to address manufacturing non-conformances.
  • Drive process improvement initiatives using SPC, Six Sigma, and Lean methodologies.
  • Ensure manufacturing processes meet operational and regulatory requirements (ISO 9001, 13485, 21 CFR Parts 210 & 211).
  • Support audits, change control, document control, and product validation.
  • Provide training and guidance on best practices and quality standards.

Requirements:

  • Degree in Business, Sciences, or Engineering.
  • 5+ years’ experience in quality operations within biotech or pharmaceutical manufacturing.
  • Strong knowledge of ISO 9001/13485 and regulatory compliance.
  • Proficiency in problem-solving tools (ASQ, Green Belt, Lean Six Sigma preferred).
  • Excellent communication, collaboration, and decision-making skills.
  • Advanced MS Office skills preferred.

Apply now in a few quick clicks

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.