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• Maintain and continuously improve the site Quality Management System in accordance with ISO 9001 requirements.
• Own and manage all quality procedures, policies and quality documentation.
• Ensure document control processes are effectively maintained and continuously improved.
• Lead Management Review activities and monitor quality performance indicators.
• Drive quality compliance across all departments.

• Own and manage the site's:
• Change Control process
• Non-Conformance process
• CAPA process
• Document Control process
• Internal Audit programme
• Ensure quality processes remain effective, compliant and fit for purpose.
• Identify opportunities to improve existing processes and implement changes where required.
• Develop new procedures and work instructions where necessary.

• Plan and conduct internal audits.
• Act as the site quality representative during customer and certification audits.
• Ensure timely closure of audit findings and corrective actions.
• Support regulatory and customer compliance activities.
• Maintain audit readiness across the site.

• Work closely with manufacturing and engineering teams to resolve quality issues.
• Lead investigations into customer complaints, non-conformances and product quality concerns.
• Drive root cause investigations and implementation of sustainable corrective actions.
• Support New Product Introduction (NPI) activities and engineering change requirements.
• Participate in risk assessments, process reviews and improvement projects.

• Monitor quality metrics and identify opportunities for improvement.
• Drive CAPA effectiveness and process improvement initiatives.
• Support Lean and Six Sigma activities where appropriate.
• Promote a culture of quality and continuous improvement throughout the organisation.

• Degree or equivalent qualification in Engineering, Quality, Manufacturing or a related discipline.
• Proven experience in a Quality Manager or Quality Lead role.
• Experience managing and improving Quality Management Systems in a manufacturing environment.
• Strong knowledge of ISO 9001.
• Experience owning or managing: Change Control, CAPA, Non-Conformance Management, Internal Audits, Document Control
• Experience writing, implementing and improving quality procedures and processes.
• Strong root cause investigation and problem-solving skills.
• Experience working directly with manufacturing and engineering teams.
• Ability to work independently with minimal supervision.

• Electronics, semiconductor, electromechanical or precision manufacturing experience.
• Experience supporting new product introduction and engineering changes.
• Internal Auditor or Lead Auditor qualification.
• Exposure to Regulatory Affairs activities.
• Lean Six Sigma certification or continuous improvement experience.
• Customer quality and supplier quality experience.

• Self-sufficient and highly autonomous.
• Comfortable making decisions without daily supervision.
• Practical and hands-on in their approach.
• Able to balance quality system requirements with manufacturing realities.
• Organised, methodical and detail focused.
• Confident communicating with customers, auditors and internal stakeholders.
• Proactive and improvement-oriented.

• Established ownership of the site Quality Management System.
• Maintained audit readiness and compliance standards.
• Improved quality processes where gaps or inefficiencies exist.
• Built strong working relationships across production and engineering.
• Driven measurable improvements in quality performance and process effectiveness.
• Become the site's recognised quality authority and primary quality contact

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.