Quality Engineer

Quality Engineer

Full-Time 36000 - 44000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Ensure top-notch quality in electronics manufacturing and promote a positive quality culture.
  • Company: Join Custom Interconnect, a leading electronics manufacturing service with a passion for excellence.
  • Benefits: Competitive salary, supportive team environment, and opportunities for professional growth.
  • Other info: Be part of a company dedicated to innovation and continuous improvement.
  • Why this job: Make a real impact in high-tech electronics while developing your skills in a dynamic setting.
  • Qualifications: 2+ years in quality engineering, experience with ISO standards, and problem-solving skills.

The predicted salary is between 36000 - 44000 £ per year.

Company Information and Introduction

At Custom Interconnect we plan to succeed and never fail! Our values dictate that we have an unrivalled passion for providing the best Electronics Manufacturing Support on offer, with an honest and open attitude to business. Our vision is to be customers' first choice for the manufacture of mission critical, high technology electronics, adding value globally, and we are dedicated to delivering innovation and service excellence by investing in design, build and fulfilment of our Customers Products. Formed in 1987, as a company CIL have grown steadily to become one of the major Electronics Manufacturing Service companies available today. Located in Andover, Hampshire, our 2 manufacturing facilities comprises 80,000sq ft of modern production space to meet our customers' needs.

Key Responsibilities and Duties

As Quality Engineer (cleanroom), you will support the development and maintenance of Custom Interconnect Limited’s (CIL) Business Management System by promoting and developing a positive Quality culture within the organisation. More specifically:

  • Supporting all other departments to ensure they remain compliant to the accreditations strategic to CIL, primarily the AS9100, ISO 9001, ISO 13485 (Medical Devices) and ISO7 cleanroom accreditations.
  • Leading product quality in both customer and production related areas, which would include containment, investigation, correction, implementation, and validation of corrective actions.
  • Assisting in the development of a Continuous Improvement culture throughout the Business.
  • Supporting the introduction of Customer led Quality Initiatives such as Total Preventative Maintenance.

Key accountabilities include but are not limited to:

  • Assist the Process Engineering team to identify and document all clean room-related procedures, SOPs and assembly instructions and review for compliance with accredited Quality Standards.
  • Developing, maintaining, monitoring, and reviewing Quality Manufacturing Plans and PFMEAs for key products.
  • Supporting the production department to ensure all control measures are followed (material expiration, training records, preventative maintenance, etc.).
  • Conducting Quality spot-checks within the production department, such as internal spot/scheduled audit of a process or team and direct inspection of work-in-progress or completed assemblies.
  • Assist Senior Management, Process Engineering and Maintenance to monitor clean room performance, monitor personnel adherence to clean room best practices, arrange and coordinate with suppliers for annual deep-clean activity and external validation of clean room performance.
  • Function as the first point of contact for all external audits including certification of the clean room to ISO7 standard in accordance with BS EN ISO 14644.
  • Establish a clean room specific calibration controls and monitor the status of all measurement equipment used within the clean room, arranging on-site calibration or items to be sent away to an external calibration house.
  • Monitor and record the performance of all temperature critical appliances in accordance with CIL procedures.
  • Establish a clean room specific tool register to actively monitor and periodically check all bespoke jigs and fixtures in production use, highlighting where tools need to be repaired or replaced.
  • Ensure all applicable substances in use within the clean room are suitably identified and present on the company COSHH register, with both TDS and MSDS documents available for review as required.
  • Review internal rejections raised by the Production team and lead investigations into cases of repeated poor product quality. Work with and assist Production and Process Engineering to identify and implement opportunities for improvement.
  • Review and monitor the accuracy of the training status of all personnel as recorded in the clean room Training Matrix, assisting Production and Process Engineering to highlight additional or improved training needs.
  • Assist Production and Process Engineering in the continual monitoring and improvement of application of 6S principles.
  • Monitor SPC data alongside engineers applying six sigma methodology to trend analysis.

Key Skills and Competencies

  • A minimum of 2 years’ experience working in a Quality Engineer role within a manufacturing/engineering environment, prior cleanroom experience is desirable.
  • Experience of working within an organisation certified to one or more of the following standards: ISO 9001, AS 9100, ISO 13485, IATF 16949.
  • Experience in problem solving and investigation tools such as 8D, CAPA, 5-Whys.
  • Experience in internal auditing to ISO 9001, AS9100D or ISO 13485.
  • Proficiency in Microsoft Office (or equivalent), data handling and analysis.
  • Demonstrable ability to communicate with internal and external stakeholders at all levels of the business.
  • Ideally educated to HNC level (Level 4) in a discipline beneficial to the Company’s needs, such as Electronics Engineering.
  • Lean Six Sigma qualified to yellow or green belt.
  • Experience in inspection, including first article inspection.

Additional Information

  • Number of positions: 1

Quality Engineer employer: HR Duo, Ltd.

HR Duo, Ltd. is an excellent employer that values teamwork and precision in the dynamic field of PCB production. Located in Andover, UK, we offer a supportive work culture that fosters employee growth through continuous training and development opportunities. Our commitment to health and safety ensures a secure working environment, making us an attractive choice for those seeking meaningful and rewarding employment in manufacturing.

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Contact Details:

HR Duo, Ltd. Recruitment Team

We think you need these skills to ace Quality Engineer

Quality Management Systems
ISO 9001
AS9100
ISO 13485
ISO14001
Cleanroom Standards
Continuous Improvement