In this role you will strengthen and evolve the Quality Management System within a pharma-manufacturing environment, partnering with internal teams and suppliers to drive quality performance. You will conduct QMS audits, investigate non-conformances, and lead root-cause analysis to close actions and improve outcomes. The position offers solid technical development and progression within a well-regarded engineering business focused on continuous improvement. This is an office-based, permanent role with a strong quality-first culture.
Pay / Benefits
25 days leave
training and technical development
progression opportunities
37.5 hours/week
Mon-Fri office-based
salary (competitive)
Responsibilities
Maintain and improve the Quality Management System to ISO 9001 and UKAS requirements
Support and conduct audits to ensure compliance and identify improvements
Investigate non-conformances and quality issues using structured RCA tools
Lead root-cause analysis using 5 Why / Fishbone / 8D and similar methodologies
Support reporting of quality metrics and assist with customer complaint investigations
Collaborate with internal teams and external customers/suppliers to drive quality performance
Key requirements
Experience in a technical, engineering, or manufacturing quality role
Working knowledge of ISO 9001 (or similar quality standard) and non-conformance management
Familiarity with corrective actions and problem-solving tools (5 Why, Fishbone, 8D, FMEA)
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