I am seeking a CMM Programmer and a CMM Inspector to join a business based in Leeds.

This company delivers high performance precision engineering solutions to the healthcare / aerospace sector. They specialise in manufacturing complex components, prototypes and production surgical instruments for medical procedures.

Job Title: CMM Programmer and a CMM Inspector

Location: Leeds (relocating to Castleford within 12 months)

Contracts: Permanent

CMM Inspector Salary: £42,000.00 + Shift Allowance Monday to Friday afternoon shift- Monday – Thursday 3pm – 11pm, Friday 2pm – 10pm

CMM Programmer Salary: £42,000.00 Monday to Friday Day shift- Monday – Thursday 7am – 3.15pm, Friday 7am – 2.30pm

In both roles, you will be reporting to the QA/RA Manager, and you will play a key role in ensuring quality standards are maintained across production through advanced metrology, inspection, and continuous improvement activities

This is an excellent opportunity to join a quality-focused manufacturer where you can make a real impact and further develop your career in a highly regulated environment.

Daily Responsibilities:

• Programme and operate Mitutoyo CMMs using MCOSMOS and CAT1000D software.
• Create and maintain CMM inspection routines ahead of production.
• Carry out first-off, in-process, and final inspections.
• Use manual inspection equipment including micrometers, verniers, height gauges, and bore gauges.
• Interpret engineering drawings, CAD models, and GD&T specifications.
• Produce inspection reports and maintain quality records.
• Support non-conformance investigations, CAPA activities, and root cause analysis.
• Maintain calibration schedules and inspection equipment.
• Assist with audits and ISO 13485 compliance.
• Train and support colleagues in inspection techniques.
• Drive continuous improvement initiatives to improve quality, efficiency, and delivery performance.

To be considered:

• Proven experience within precision engineering.
• Strong knowledge of MCOSMOS software and CMM best practices.
• Excellent understanding of GD&T and technical drawings.
• Experience with ISO 13485, ISO 9001, or similar quality systems.
• Familiar with NCRs, CAPA, FAIRs, and quality documentation.
• Strong attention to detail and problem-solving skills.
• Comfortable working across production, engineering, and quality teams.

Desirable

• Medical device manufacturing experience.
• Knowledge of MICAT software.
• Experience with Lean and continuous improvement methodologies.

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