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Quality Engineer

Job Posted: 6 hours ago

  • Salary: £ 35,000 - 41,000 / Annum

    Job Type: Permanent

  • Location: Bacup, Lancashire

Expire in: a month

Job Description

QUALITY ENGINEER Location: Lancashire Hours: 35 hours per week (Mon–Thu 08:30–17:00, Fri 08:30–13:30) Industry: Medical Devices / Advanced Manufacturing About The Role Are you a meticulous, motivated Quality Engineer looking to make a real impact in a growing, high-tech medical manufacturing environment? We are a leading producer of orthopedic components and polymeric materials, supplying high-specification products to the medical industry worldwide. With ongoing business growth, we are seeking a skilled Quality Engineer to join our expanding Quality Department. This is an exciting opportunity to contribute to world-class manufacturing standards, support innovation, and help drive continuous improvement across our operations. Role and Responsibilities * Making risk-based decisions to drive product and process quality. * Leading and supporting root cause analysis (RCA) and CAPA activities. * Mentoring Quality Controllers and Inspectors, providing training and coaching. * Leading process improvement, validation activities, and Lean initiatives. * Designing and conducting MSA, Gauge R&R, sampling plans, and capability studies. * Interpreting customer requirements and ensuring full compliance. * Preparing clear and insightful quality metrics and reports for management. * Developing PFMEAs, risk assessments, engineering change controls and documentation. * Supporting New Product Introduction (NPI) projects. * Liaising with customers and leading escalations when required. * Conducting internal and supplier audits to ISO and customer standards. * Ensuring promotion of quality and regulatory awareness across the company. What You Need toSucceed * Qualification in Quality or Mechanical Engineering (ONC/HNC/Degree) or equivalent. * Experience in a Quality-focused role within medical, automotive, or similar regulated industries. * Strong working knowledge of QMS principles and standards (ISO 9001, ISO 13485, ISO 17025, ISO 14001, ISO 45001, FDA QSRs, MDD). * Skilled in FMEA, root cause analysis, Lean/Six Sigma tools, and process flows. * Competent in Process Validation, MSA, and Gauge R&R. * Able to interpret complex technical drawings. * Internal auditing experience to recognised standards. * Methodical, conscientious, and an effective communicator. * Excellent time-management and the ability to multitask. * Strong written communication and computer literacy. What's in it for You? * Work with cutting-edge materials and technologies in the medical sector. * Contribute to life-changing products that support patient well-being globally. * Be part of a supportive, technically strong team with opportunities to grow. * Enjoy a balanced 35-hour working week with an early finish every Friday

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