Job description

• Maintain and improve QMS within a regulated manufacturing environment
• Oversee document control, deviations, CAPAs, and change management processes
• Support batch review and product release activities
• Conduct internal audits and assist with external and regulatory audits
• Lead investigations relating to quality issues, non-conformances, and complaints
• Drive continuous improvement initiatives across the business
• Provide training and guidance to operational teams on quality standards

• Degree-qualified in Science, Life Sciences, or a related discipline
• Proven experience in a GMP-regulated environment
• Strong understanding of quality systems, compliance, and regulatory requirements
• Experience managing investigations and root cause analysis
• Excellent communication and stakeholder engagement skills
• Ability to manage competing priorities in a fast-paced setting

• Competitive salary based on experience
• Flexible start times (Monday to Friday)
• Opportunity to influence and improve systems in a growing organisation
• Supportive and collaborative team environment

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV to , or call Dave on 0477551369 now.

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