Muradiye Fidan
About Muradiye Fidan
Muradiye Fidan is a regulatory affairs specialist currently working at Boston Scientific. She has extensive experience in quality and regulatory roles across various companies in the pharmaceutical and medical device industries.
Current Role at Boston Scientific
Muradiye Fidan has been employed at Boston Scientific since 2019, serving as a Spécialiste Affaires Réglementaires. Her role involves handling regulatory affairs related to the company's medical devices and ensuring compliance with various regulations and standards.
Previous Experience at Baxter International Inc.
In 2018, Muradiye Fidan worked at Baxter International Inc. as an Assistante Charte VM. She held this position for 5 months in Guyancourt, Île-de-France, France. During her time at Baxter International, she assisted with the company's charte VM initiatives, focusing on regulatory and compliance matters.
Role at LEO Pharma A/S
Between 2016 and 2018, Muradiye Fidan was employed at LEO Pharma A/S in Voisins-le-Bretonneux. Her role involved handling quality assurance and pharmaceutical affairs, ensuring that the company's products met all relevant quality standards and regulatory requirements.
Employment at MicroVention
In 2015, Muradiye Fidan worked at MicroVention for 3 months in the capacity of Qualité - Affaires Réglementaires. Her responsibilities included ensuring regulatory compliance and maintaining quality assurance processes for the company's medical products.
Experience at PAGO – Labels & Labelling Technology
Muradiye Fidan spent a significant part of her career at PAGO – Labels & Labelling Technology. From 1998 to 2011, she held the position of Responsable Qualité in Elancourt. In this role, she was responsible for overseeing the quality assurance processes associated with the company's labeling and labelling technology products.