Quality Improvement Engineer
- AB, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Experience
- Minimum 7+ years’ experience in a Quality / Manufacturing Engineering role
- Posting language
- English
- Posted
Original job description
We are seeking an experienced and driven Quality Improvement Engineer to support ongoing operational excellence and compliance within our manufacturing environment. This role will focus on driving quality improvements, strengthening process capability, and ensuring alignment with regulatory and customer requirements, particularly within the medical device sector.
This is a hands-on, shop floor–focused role, working closely with production teams and overseeing the end-to-end machining process to ensure product quality is effectively managed, controlled, and continuously improved. The role also has a strong customer focus, supporting the resolution of customer issues and helping to build confidence through robust quality performance.
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Inspection department at Kirkstall Precision
Key Responsibilities
- Maintain a strong shop floor presence, overseeing machining processes to ensure product quality is controlled at source
- Lead and support root cause investigations using structured problem-solving methodologies (e.g. 8D, DMAIC, 5 Whys)
- Drive continuous improvement activities to reduce defects, scrap, and rework
- Analyse manufacturing data to identify trends, variation, and improvement opportunities
- Support and develop process validation activities (IQ/OQ/PQ) where required
- Apply statistical techniques (SPC, Cp/Cpk, MSA, etc.) to improve process capability and control
- Ensure compliance with ISO 13485 and relevant regulatory requirements
- Support internal and external audit activities, including customer and regulatory audits
- Work cross-functionally with Production, Engineering, and Quality teams to implement sustainable improvements
- Develop and improve standard operating procedures (SOPs) and quality documentation
- Contribute to strengthening the Quality Management System (QMS)
- Deliver quality awareness sessions and training to site teams to improve understanding and promote a strong quality culture
- Support customer issue resolution and help improve overall customer satisfaction and OTIF performance
- Minimum 7+ years’ experience in a Quality / Manufacturing Engineering role
- Strong problem-solving capability, with a structured and data-driven approach
- Proven experience in data analysis and statistical methods (SPC, Minitab or equivalent)
- Solid understanding and practical application of ISO 13485
- Experience within the medical device industry (highly desirable)
- Strong regulatory awareness and understanding of compliance requirements
- Ability to lead and influence cross-functional teams
- Excellent communication and stakeholder management skills
- Experience in CNC machining / precision manufacturing
- Knowledge of validation processes and equipment qualification
- CMM experience and familiarity with geometric/variable measurement techniques
- Familiarity with aerospace or other regulated industries (beneficial)
- Proactive and results-driven
- Detail-oriented with a strong focus on quality and compliance
- Comfortable working in a hands-on, shop floor environment
- Able to operate effectively in a fast-paced, evolving environment
- Strong team player with the ability to challenge and influence constructively
- This role offers an excellent opportunity to gain deep exposure to the business, its processes, and customers. It provides a strong platform for future career development and progression within the organisation, opening up wider opportunities as the business continues to grow.
This is a key, hands-on and customer-focused role within the business, with a strong shop floor presence, providing the opportunity to make a significant impact on product quality, process control, regulatory compliance, and customer satisfaction, while supporting future growth and operational scale.
To apply: Email your CV and three reasons you are interested in working for us to: info@kirkstallprecision.co.uk
More about this job
Responsibilities
Oversee machining processes on the shop floor and lead data-driven investigations and improvement initiatives to reduce defects, scrap, and rework while strengthening process capability. Maintain regulatory compliance and quality documentation, support audits and customer issue resolution, and work with production and engineering teams to improve quality and customer satisfaction.
Requirements
Requires at least seven years of experience in quality or manufacturing engineering, strong structured problem-solving and data-analysis skills, and practical knowledge of ISO 13485 and regulatory compliance. Medical device experience is highly desirable; CNC machining, validation, equipment qualification, and CMM measurement experience are additional advantages.
Skills
- Root Cause Analysis
- 8D Problem Solving
- DMAIC
- 5 Whys
- Continuous Improvement
- Manufacturing Data Analysis
- Statistical Process Control
- Process Capability Analysis
- Minitab
- Process Validation
- ISO 13485 Compliance
- Quality Management Systems
- Audit Support
- CNC Machining
- Precision Manufacturing
- Cross-Functional Leadership
Visa sponsorship
Not detected in the job text
Categories
- Engineering
- Manufacturing
- Healthcare
- Management & Leadership
Keywords
- Medical Device Manufacturing
- Orthopaedic Instruments
- Implants
- Quality Improvement
- Operational Excellence
- ISO 13485
- Regulatory Compliance
- Root Cause Investigation
- 8D
- DMAIC
- 5 Whys
- Continuous Improvement
- Statistical Process Control
- SPC
- Cp/Cpk
- Measurement System Analysis
- MSA
- Minitab
- Process Validation
- IQ/OQ/PQ
- Quality Management System
- QMS
- Standard Operating Procedures
- SOPs
- Internal Audits
- Customer Audits
- CNC Machining
- Precision Manufacturing
- CMM
- Geometric Measurement