Selçuk Haydanlı, who completed his undergraduate education in Pharmacy in 2002, continues to serve the sector as a Quality Management Representative within the body of Waco Biomedical & Laboratory with foreign trade, purchasing and sales, quality management systems, clinical data evaluation, post-market surveillance and customer complaints evaluation, determination and implementation of medical device production line quality control points, production and product development, production planning, operation of quality management systems and production according to ISO 13485: 2016 and ISO 9001: 2015 standards, CE certification processes, installation and requirements of HVAC (Heating Ventilating and Air Conditioning) systems experience in the medical device industry for 18 years.

After completing undergraduate education at TOBB ETU Biomedical Engineering, she has been started her career in the medical device industry with quality management systems and CE certification areas and gained experience in the requirements of becoming a medical device manufacturer. In active business life, she continues to provide services in the field of medical device as a Quality Assurance Specialist within Waco Biomedical & Laboratory with her experience in preparing technical files, operating ISO 13485: 2016 Quality Management Systems, risk analysis, process management, validations and biocompatibility assessments.

After completing undergraduate education with third place in the department, she has been started her career in the manufacturing department in the medical device industry. She continues to serve the industry as a Production Manager within Waco Biomedical & Laboratory, specializing in fields that production and product development, production planning, establishment and maintenance of production traceability system, establishment and maintenance of production in accordance with ISO 13485: 2016 Quality Management Systems, installation and requirements of HVAC (Heating Ventilating and Air Conditioning) systems, process and clean room validations.