About The QA Dr

I have a Bachelors Degrees in Pure Mathematics and Applied Chemistry respectively, a Masters in Physical Chemistry, and a Doctorate in Chemistry (The Colour of Red Wine).

My background in chemistry includes research and development in various industries such as food colourings and flavourings, (the carbonation of) concrete, wood preservation, (water management in) fuel cells, and developing novel printing inks. I have worked in the UK and Canada as an Industrial Chemist.

As a quality assurance (QA) specialist, I have worked across different fields such as biotechnology (pre-clinical and clinical trials), manufacturing (manufacturing fibre-glass nuts and bolts, and industrial-scale water purification systems), to software requirements.

Examples of the quality systems and specifications I have worked with include the OECD (Organisation for Economic Co-operation and Development) Guidelines for Good Laboratory Practice (GLP) and Good Clinical Practice (GCP), ISO 9001:2015 Quality Management Systems, as well as ISO/IEC 17025: 2017 (Testing and calibration) and ISO/IEC/IEEE 29148:2018 (Systems and software engineering — Life cycle processes — Requirements engineering).

In response to growing demand, I am expanding my focus to specialise in technical writing. My ability to translate complex concepts into clear, actionable documentation has proven invaluable across various industries, particularly in IT projects such as system migrations and cloud transitions.

This shift allows me to leverage my expertise in creating structured, user-friendly materials that support both technical teams and end-users. Whether it’s developing policies, procedures, or comprehensive reports, I am committed to delivering documentation that drives understanding, efficiency, and success.