Job Description

Location Worthing


Discipline: Quality Assurance


Job type: Permanent Full Time


Job ref: 010947



We're seeking a Quality Engineer who thrives on collaboration and precision. In this role, you will play a key part in ensuring the highest standards across our processes, working closely with cross-functional teams to drive continuous improvement and deliver exceptional results.





Quality Engineering at Rayner plays a crucial role in delivering high quality and high performance medical devices to people around the world. It ensures our quality standards are rigorous and robust processes, built into manufacturing at every step from raw material inspection to final product release. Through continuous improvement and teamwork we continue to excel and meet this goal together.

What You'll Be Doing:

Initiate and lead CAPA investigations with cross-functional teams including Production and Process Engineering to deliver defect reduction Drive process and continuous improvement in Manufacturing to improve quality and efficiency of receiving inspection and in-line process checks Manage non-conformity and supplier activities to ensure compliance and improve performance Work with suppliers to maintain performance and align quality standards for incoming materials (Right First Time) Build effective working relationships with colleagues and suppliers Monitor, trend and report on quality performance data to track KPIs Assist the Head of Quality and Quality Engineering team with Supplier and internal process audits Support new product and process development projects Actively promote a Quality culture within Rayner and throughout the supply chain

What Experience & Skills You Will Need:

Competencies:


Excellent ability in managing people and projects for CAPA and process improvement Able to communicate effectively and build relationships at all levels of a company Capable in investigating and effectively solving complex issues using methodologies and root cause analytical tools such as 8D, Fishbone Diagram, FMEA, 5 Whys Excellent oral, written and presentation skills Proficient with data analysis, reporting and monitoring KPIs Familiar with using databases and business management systems (ERP/eQMS) Competent in industry standard IT practices and use of Microsoft applications

Requirements:


Proven track record of process improvement experience resulting in better quality, cost, efficiency and time within a manufacturing environment Degree, equivalent qualification, or equivalent industrial experience in a science, clinical or engineering background 2-3 years' experience in a Quality Engineering role Experience with Quality System concepts, practices and procedures Experience working in a high volume, fast-paced manufacturing setting (desirable) Working knowledge of standards such as cGMP, FDA 21 CFR Part 820 QSR and ISO 13485 Medical Device Quality Management Systems (desirable)

What We Can Offer You:

On-site Restaurant for affordable, convenient meals Private Healthcare (access to remote GP & Counselling) for peace of mind Monthly Massages to relax and recharge On-site Parking for convenience and cost efficiency Annual Wellbeing Reimbursement to care for your mind and body Pension Plan to secure your future Cycle-to-work Scheme to stay active and eco-friendly Enhanced Parental Pay to support new families * Referral Bonus to benefit from recommending talent