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Senior Quality Assurance Manager

2 months ago


Livingston, West Lothian, United Kingdom Kleboe Jardine Ltd Full time

About Kleboe Jardine Ltd

Kleboe Jardine Ltd is a well-established company in the medical device industry, with a strong presence in the global market. Our company has a rich history of innovation and excellence, and we are committed to delivering high-quality products to our customers.

Job Summary

We are seeking a highly skilled and experienced Senior Manufacturing Quality Engineer to join our Quality team. The successful candidate will be responsible for developing and implementing quality metrics, analyzing data and trends, and leading quality improvement projects.

Key Responsibilities

  • Quality Metrics and Planning
    • Develop and collate quality metrics to measure product and process performance
    • Produce quality plans for existing products and processes
  • Data Analysis and Trending
    • Analyze data and trends in performance and variation of products, processes, and non-conformance reports
    • Use statistical methods to identify areas for improvement
  • Quality Improvement and Continuous Improvement
    • Lead and facilitate quality improvement projects in partnership with Manufacturing and Engineering teams
    • Collaborate with cross-functional teams to identify and implement process improvements
  • Risk Management and FMEA
    • Facilitate risk management activities, including FMEAs
    • Ensure that risk management activities are aligned with company policies and procedures
  • Technical Documentation
    • Write and review technical documents, including standard operating procedures and work instructions
    • Ensure that technical documents are accurate, complete, and compliant with regulatory requirements
  • Coaching and Guidance
    • Provide coaching and guidance on quality topics to Production and Engineering teams
    • Develop and deliver training programs to improve quality awareness and skills
  • Audit and Compliance
    • Conduct internal audits to ensure compliance with quality policies and procedures
    • Identify and implement corrective actions to address audit findings

Requirements

  • Experience
    • Minimum 5 years of experience in a quality assurance role in the medical device industry
  • Skills and Qualifications
    • Excellent analytical and problem-solving skills
    • Strong communication and interpersonal skills
    • Ability to work independently and as part of a team
    • Proficient in quality tools and techniques, including FMEA and statistical process control

About the Role

This is an exciting opportunity to join a dynamic and innovative company that is committed to delivering high-quality products to our customers. The successful candidate will have the opportunity to work with a talented team of professionals and contribute to the company's continued success.