Andrew Killick Email & Phone Number

Wellingborough, Gb

• Lead the development and continual improvement of processes for the QMS (ISO 13485:2016)• Manage quality issues, such as complaints, deviations, and non-conformances ensuring thorough investigations• Ensure quality control procedures are established and executed in accordance with customer requirements • Organize and support audits to ensure ISO compliance• Collaborate with cross-functional teams to resolve quality issues and implement corrective measures• Manage non-conforming products, perform/support root cause analysis, and drive corrective actions• Plan, develop, perform validation activates (Equipment Qualification, Computer System Validation, & Process Validation)• Collaborate with cross-functional teams to evaluate and select suppliers on quality requirements• Monitor supplier performance and implement improvement plans, as necessary• Execute competency reviews, maintaining training records as necessary in order to optimise information management• Participate/Lead management review meetings to assess the effectiveness of the QMS• Lead and facilitate continuous improvement initiatives to enhance operational efficiency and product quality • Ensure accurate and timely documentation of quality related activities, including corrective actions and change controls• Monitor and maintain the equipment asset register and associated activities to ensure all equipment is suitable for its assigned tasks and undergoes regular checks and maintenance/calibration• Ensure all quality documentation is followed, adhered to and maintained• Perform Failure Mode and Effect Analysis (FMEA) risk assessments

Bedfordshire, England, United Kingdom

Creonate Manufacturing - formerly Global Access Diagnostics (GAD)• Validation of equipment used to manufacture lateral flow medical device tests• Develop validation master plans• Perform Failure Mode and Effect Analysis (FMEA) assessments • Develop data analysis tools & methodology for equipment validation• Develop, monitor and update a validation tracking system• Lead continuous improvement actives within the Creonate validation team• Create and update validation and manufacturing SOP’s• Execution of quality processes; nonconformities, deviations, change control, risk assessment and implementation plans• Liaise between Creonate departments to ensure validation protocols are executed effectively • Execution of factory acceptance tests (FAT) alongside equipment suppliers • Assist heath and safety in dynamic risk assessments of equipment

Bedfordshire, England, United Kingdom

• Assist in equipment validation activates • Perform Failure Mode and Effect Analysis (FMEA) assessments

Bedfordshire, England, United Kingdom

• Manufacturer lateral flow medical device tests – primary focus on COVID-19 test devices• Create and implement manufacturing standards• Technical transfer between R&D and manufacturing• Lead continuous improvement activities• Develop data analysis tools & methodology• Manage machine operators to achieve production targets• Coordinate training for machine operates• Liaise production & continuous improvement activities to all levels of staff• Quality check manufactured components

Bedfordshire, England, United Kingdom

• Liaise between GAD and the Toyota continuous improvement team• Support and lead continuous improvement actives within the GAD manufacturing team, resulting in reduced training times for new staff and material wastage.

Bedfordshire, England, United Kingdom

• Manufacturer lateral flow medical device tests – primary focus on COVID-19 test devices• Create and implement manufacturing standards• Quality check manufactured components

Northampton, United Kingdom

• Process semiconductor wafers through a number of automated and manual tools/processes. • Supervise laboratory processes during out of hours shift. • Provide full technical support to the Epitaxy management. • Perform manufacturing activities according to process instructions. • Ensure the continued widening of job knowledge to include all upcoming products. • Observe and adhere necessary workplace disciplines and safety procedures. • Set up, adjust, and operate a variety of complex computer controlled equipment involved in the manufacture of photonic devices and other related products. • Operate as the department’s fire marshal.

• Provided mainly international, Non-English speaking students with academic support and assistance. • Mentored and supported 2 international students - facilitated their understanding of RTL design with FPGA design tools and Verilog, semiconductor devices and device physics, state machines, and CMOS / NMOS technology and physical layout.

• Assisted service users with various chores, including medication preparation. • Focused on the mental stimulation and general well-being of service users.

Aided understanding of soldering, wiring, machining, and circuit planning and implementation.

Master'S Degree, Microelectronic Systems Design, Distinction

This course was focused on the design, fabrication and testing of microelectronic devices. Modules included Project Management, Dynamic.

Bachelor'S Degree, Electronics, Beng (Hons) Electronics

In the first year of this course I developed a firm understanding of the fundamentals of electronics, with modules in Electronic circuits.

Btec National Diploma, Engineering, Ddm

City & Guilds, Engineering Principles, Cq