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Quality Engineer

Meriden Media

Retford

On-site

GBP 35,000 - 42,000

Full time

16 days ago

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Job summary

An established industry player is seeking a Quality Engineer to enhance quality processes and ensure compliance with industry standards. In this role, you will collaborate with various teams to drive continuous improvement and manage quality investigations. Your expertise will be crucial in implementing corrective actions and supporting audits while ensuring that manufacturing processes adhere to regulatory requirements. If you have a passion for quality assurance and a strong background in biotech or pharmaceutical manufacturing, this opportunity is perfect for you to make a significant impact in a dynamic environment.

Qualifications

  • 5+ years' experience in quality operations within biotech or pharmaceutical manufacturing.
  • Strong knowledge of ISO 9001/13485 and regulatory compliance.

Responsibilities

  • Lead quality investigations for market defects and implement corrective actions.
  • Drive process improvement initiatives using SPC, Six Sigma, and Lean methodologies.

Skills

Problem-solving
Communication
Collaboration
Decision-making

Education

Degree in Business
Degree in Sciences
Degree in Engineering

Tools

ASQ
Lean Six Sigma
MS Office

Job description

Quality Engineer

Up to £42k DOE

Monday - Thursday 07:00 - 16:00, Friday 07:00 - 13:00

Seeking 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:

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

Requirements:
  1. Degree in Business, Sciences, or Engineering.
  2. 5+ years' experience in quality operations within biotech or pharmaceutical manufacturing.
  3. Strong knowledge of ISO 9001/13485 and regulatory compliance.
  4. Proficiency in problem-solving tools (ASQ, Green Belt, Lean Six Sigma preferred).
  5. Excellent communication, collaboration, and decision-making skills.
  6. Advanced MS Office skills preferred.
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