R&D Scientist at ADVANCED MEDICAL SOLUTIONS (2026-03 – Present)
- Conduct viscosity testing to evaluate material flow characteristics and product performance.
- Perform set time testing to determine curing and polymerisation characteristics of medical adhesive formulations.
- Carry out set time assessments on pig skin models to evaluate product performance under simulated biological conditions.
- Conduct tensile testing to assess mechanical strength and material durability.
- Perform T-peel testing to evaluate adhesive bond strength and peel resistance.
- Conduct Karl Fischer titration to determine moisture content and support material and product quality assessment.
- Prepare samples, record experimental data, analyse results, and generate technical reports.
- Support product development, formulation optimisation, and verification activities within the R&D department.
- Maintain laboratory equipment and ensure compliance with laboratory procedures, quality standards, and safety requirements.
- Written and executed 3 study protocols for performance and stability testing since joining the company.
Research Officer at THE INSTITUTE OF METAL RESEARCH (NAAIMCAS) (2024-01 – 2025-08)
- Quality Documentation: Authored peer-reviewed technical publications and contributed to strategic project proposals requiring high data integrity.
- Coordinated international research collaborations, accelerating knowledge exchange and positioning the institute for future funded projects.
- Translated experimental data into high‑quality technical reports and peer‑reviewed publications used to support strategic research planning.
- Supported proposal development by synthesizing literature, experimental results, and impact statements aligned with funder priorities.
- Delivered clear presentations to internal and external stakeholders, improving decision‑making around materials research directions.
R&D Scientist – Medical Devices & Biomaterials at UNIVERSITY OF SCIENCE AND TECHNOLOGY CHINA (2019-01 – 2023-12)
Biomaterials Laboratory
- Designed, tested, and optimised nanoparticle‑based surface coatings for polymeric and biodegradable ureteral stents, focusing on reproducible antibacterial performance and biocompatibility under controlled experimental conditions.
- Executed full R&D testing cycles, from materials synthesis and surface modification through iterative in‑vitro testing, protocol optimisation, and performance verification.
- Generated statistically robust and reproducible datasets to evaluate microbial adhesion, surface performance, and biological response, supporting product‑relevant decision‑making.
- Collaborated closely with engineers and clinicians to align test methods, performance metrics, and reporting with real‑world device and clinical requirements.
Masters Researcher at NORTHEASTERN UNIVERSITY (2016-01 – 2019-12)
- Supported applied biomaterials research through rigorous data analysis, repeatability checks, visualisation, and structured technical reporting.
- Improved data presentation workflows, enabling faster interpretation and publication readiness.
- Assisted postgraduate researchers with experimental planning, manuscript editing, and quality control.
Operations Manager at BEDEEN CLEANING SERVICES (2025-09 – 2026-02)
Transferable Impact: Demonstrates strong operational discipline, cost control, stakeholder management, and process optimization relevant to industrial R&D settings.
- Manage day‑to‑day operations, scheduling, procurement, and budget control in a fast‑paced service environment.
- Implemented structured record‑keeping and audit processes, improving data accuracy and operational transparency.
- Act as primary client liaison, conducting site audits and performance reviews to maintain service quality.
Laboratory Assistant at ROTAN MEDICAL DIAGNOSTIC CENTRE (2013-01 – 2016-12)
Outcome & Impact: Maintained consistent analytical accuracy while ensuring full compliance with laboratory safety and infection‑control standards.
- Prepared, labelled, and processed samples while maintaining strict biosafety, infection-control, and quality standards.
- Recorded, verified, and organised test data to support clinical reporting and traceability.
- Managed laboratory consumables and inventory, ensuring uninterrupted laboratory operations.
- Adhered consistently to health, safety, and regulatory requirements within a laboratory environment.
