We are seeking an experienced and motivated Quality Engineer to join a growing medical device business on an initial 6 month contract.
The following information aims to provide potential candidates with a better understanding of the requirements for this role.
This is an exciting opportunity to play a key role in maintaining and improving quality systems that support the development and manufacture of innovative medical technologies that positively impact patient outcomes worldwide.
Working closely with cross-functional teams including Manufacturing, R&D, Regulatory Affairs, and Supply Chain, you will help ensure products consistently meet regulatory, customer, and business requirements.
Key Responsibilities
Support and maintain the Quality Management System (QMS) in compliance with ISO 13485, FDA QSR, and applicable regulations.
Lead investigations into non-conformances, deviations, complaints, and CAPAs.
Conduct root cause analysis and implement effective corrective and preventive actions.
Support internal, supplier, and external audits, including regulatory inspections.
Review and approve quality documentation, including procedures, work instructions, and validation reports.
Drive continuous improvement initiatives across manufacturing and operational processes.
Support risk management activities in line with ISO 14971.
Monitor quality metrics and identify opportunities for improvement.
Work closely with suppliers to ensure material and component quality standards are maintained.
Participate in design transfer, validation, and product lifecycle quality activities.
About You
You will be a proactive quality professional who thrives in a regulated environment and is passionate about delivering high-quality medical devices.
Essential Requirements:
Degree in Engineering, Science, Quality, or a related discipline.
Experience in a Quality Engineering or Quality Assurance role within the medical device, pharmaceutical, or highly regulated industry.
Understanding of ISO 13485 and medical device quality requirements.
Experience managing CAPAs, non-conformances, and root cause investigations.
Knowledge of risk management and validation activities.
Excellent communication and stakeholder management skills. xsabvtc
Strong analytical and problem-solving abilities.
Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy...
Quality Engineer in Longridge employer: SRG
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