Ayline Yudhira is a seasoned Belgian professional with a strong track record in the medical device industry and clinical trial experience in the pharmaceutical and biotech sectors.

She brings deep expertise in aspects of MD product lifecycle management ranging from R&D, clinical development to post market surveillance requirements all whilst ensuring regulatory compliance throughout geographic market expansion strategies. She developed this expertise through senior roles at innovative companies working with disruptive technologies such as 3D additive manufacturing and neuromodulation.

In the biotech industry, she led global clinical trial teams as a Quality and Risk Manager successfully through regulatory inspections. In addition to her leadership roles, Ayline is an experienced trainer, sharing her knowledge through tailored learning programs that empower teams to navigate regulatory and quality frameworks with confidence.

Ayline has successfully led cross-functional teams and driven departmental transformations, enabling organizations to implement sustainable, end-to-end processes that deliver meaningful healthcare solutions to patients, caregivers, and medical professionals. A firm believer in the power of open dialogue and thoughtful leadership, she is known for her collaborative approach—connecting expertise across disciplines and translating strategic product roadmaps into effective day-to-day execution.

Her professional journey began in clinical care, with a background as a Geriatric Nurse. Guided by her lifelong belief that “the elderly are the future,” she earned a Master’s degree in Nursing Sciences with a specialization in Geriatrics (2006), followed by an Advanced Master in Bioethics (2019), further deepening her commitment to ethical and patient-centred innovation in healthcare.