Role Purpose: To support the transition of in vitro diagnostic (IVD) products from R&D into scalable manufacturing by executing and improving development-scale production processes. The Development Technician will work closely with R&D scientists, engineers, and manufacturing personnel to ensure that processes are robust, reproducible, and compliant with quality and regulatory standard The Manufacturing / Development Technician will work closely with R&D scientists, engineers, and manufacturing personnel to ensure that processes are robust, reproducible, and compliant with quality and regulatory standards. Key Responsibilities: · Set up, operate, and troubleshoot equipment and instrumentation on the development manufacturing line. · Perform technical tasks such as reagent mixing, filling, cartridge assembly, functional testing, and packaging in accordance with batch records and protocols. · Record experimental and manufacturing data accurately, including completion of batch documentation and deviation logs. · Assist engineers and scientists in trialling and optimizing manufacturing processes and equipment. · Provide feedback on process issues and opportunities for improvement based on hands-on experience. · Work in compliance with Good Manufacturing Practice (GMP), ISO 13485, and other relevant standards. · Participate in investigations, root cause analysis, and CAPAs for process deviations or non-conformances. · Support validation activities including IQ/OQ/PQ and documentation generation. · Collaborate with R&D, Quality and Engineering teams to support the development and launch of new diagnostic tests. Required Qualifications & Experience: Essential: · GCSE/A level qualifications · Ability to use Microsoft software packages Desirable: · Experience in a regulated manufacturing or laboratory environment (ideally within IVD, medical device, or pharmaceutical /Production sectors). · Hands-on experience with technical equipment, instrumentation, or diagnostic product assembly processes. · Prior involvement in process development or pilot manufacturing activities. · Knowledge of ISO 13485, cGMP, or FDA QSR requirements. · Experience with lean manufacturing tools or continuous improvement initiatives. Key Competencies & Behaviours: · Attention to Detail: Accurate completion of technical tasks and documentation. · Problem Solving: Ability to identify issues, perform basic troubleshooting, and contribute to process improvements. · Teamwork: Willingness to work flexibly in a cross-functional team environment. · Technical Aptitude: Strong mechanical or process understanding with a willingness to learn new equipment and procedures. · Initiative: Proactive in seeking improvements, raising concerns, and suggesting solutions. Working Conditions: · Primarily laboratory and controlled manufacturing environment. · May involve shift work or flexible hours to support development timelines. · Use of PPE and adherence to safety protocols required.