A dedicated and ambitious Quality Assurance professional, she has built a strong career within the medical devices sector, progressing from quality control leadership into a comprehensive quality assurance role. Known for her analytical mindset, attention to detail, and ability to quickly master new systems and standards, she plays a key role in maintaining and continuously improving a regulated Quality Management System aligned with ISO 13485 and MDR/MDD requirements. Her experience spans internal auditing, complaint and non‑conformance management, sterilisation release, bioburden testing, calibration oversight, and the development of robust inspection and labelling processes. She brings a calm, structured, and solutions‑focused approach to complex quality challenges, ensuring compliance while supporting operational efficiency.

With a background that includes supervising quality control teams, developing inspection protocols, managing supplier‑related issues, and driving improvements through data‑led decision‑making, she combines hands‑on technical expertise with strong leadership capability. She is confident working cross‑functionally, adept at training and developing others, and experienced in managing documentation, workflows, and controlled processes in a fast‑paced manufacturing environment. Motivated by continuous growth and professional development, she is now seeking a new opportunity that will allow her to apply her quality expertise more broadly while further advancing her skills within a forward‑thinking organisation.

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