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Quality Engineer

3 months ago

Livingston, United Kingdom Kleboe Jardine Ltd Full time

The opportunity has arisen for an experienced Senior Manufacturing Quality Engineer , to join a well-established Medical Device Company in Livingston. Our client is a leading manufacturer of sterile injectables used in various medical procedures.


The business has contributed to global healthcare for 25+ years and is a part of global group leading in the optical and optoelectronics industries.


The business has recently experienced a period of expansion and is positioning itself for further growth. We are recruiting a talented, dynamic, and self-motivated individual to join the existing Engineering team.


The Senior Manufacturing Quality Engineer will be a talented, dynamic and self-motivated individual who will contribute to the existing Quality team.


Responsibilities

  • Develop and collate quality metrics, and produce quality plans for existing products and processes
  • Analyse data and trends in performance/variation of the product, process, non-conformance reports and corrective and preventative actions using appropriate analysis methods
  • Lead/facilitate quality improvement, and continuous improvement projects in partnership with Manufacturing and Engineering
  • Facilitate risk management activities including facilitating and maintaining FMEAs
  • Write and review technical documents, including standard operating procedures and work instructions
  • Ensure integrity of process quality and source inspections
  • Provide coaching and guidance on quality topics to the Production and Engineering teams
  • Member of internal audit team - conducting process, product, and workplace audits


Applicant requirements

  • Experience in Medical Device, Pharma, Biotech or a heavily regulated industry
  • Excellent analysis of data and reporting, including graphical and statistical methods
  • Excellent problem solving and decision making skills
  • Proficient in the use of quality tools and techniques
  • Demonstrated ability to write and review technical documents
  • Proven ability to work as part of a team, independently and to earn the trust of stakeholders


This is a fantastic opportunity to join the Quality team of an established leader in the medical device and optical space. Apply as directed above, or contact Campbell Pratt | for a confidential discussion.