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Quality Engineer
2 months ago
The opportunity has arisen for an experienced Senior Manufacturing Quality Engineer, to join a well-established Medical Device Company in Livingston. Our clientis a leading manufacturer of sterile injectables used in various medical procedures.
Find out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now.
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 | cp@kleboejardine.com for a confidential discussion.