Marylène Dubois
About Marylène Dubois
Marylène Dubois is a Quality Assurance Specialist for Europe at Stepan Company, with over 15 years of experience in the pharmaceutical and medical devices industries. She has held various roles in analytical development and quality control across several companies in France.
Current Role at Stepan Company
Marylène Dubois serves as a Quality Assurance Specialist for Europe at Stepan Company, a position she has held since 2021. Based in Voreppe, France, she focuses on ensuring compliance with quality standards and regulations within the company's operations. Her role involves implementing Good Manufacturing Practices (GMPs) and maintaining Quality Management Systems (QMS) to support the production of high-quality products.
Previous Experience in Pharmaceutical Development
Marylène Dubois has extensive experience in the pharmaceutical sector, having held various positions prior to her current role. She worked as a Pharmaceutical Development Study Leader at Aguettant Laboratories for two months in 2013. Additionally, she served as an Analytical Development Project Leader at Famar from 2012 to 2013, and as an Analytical Development Manager at Patheon from 2013 to 2017. Her roles involved overseeing analytical methods and ensuring product quality throughout the development process.
Educational Background in Chemistry
Marylène Dubois studied at ENSCT / ENSIACET, where she earned a degree in Chemistry and became a Chemical Engineer. Her education spanned from 2000 to 2003, providing her with a solid foundation in chemical principles and practices that she applies in her professional roles within the pharmaceutical and medical device industries.
Expertise in Quality Assurance and Regulatory Compliance
With over 15 years of experience in the pharmaceutical and medical devices industries, Marylène Dubois possesses a strong focus on chemical analyses, including chromatography, spectrometry, and dissolution. She is skilled in applying Good Manufacturing Practices (GMPs) and ensuring data integrity. Her expertise encompasses various regulations related to medicines and medical devices, including documentation, Quality Management Systems (QMS), Corrective and Preventive Actions (CAPA), and investigations.
Career Opportunities and Preferences
Marylène Dubois is open to exploring positions related to laboratory or quality assurance departments, particularly in research and development (R&D) or production activities. She is interested in roles that may involve team management responsibilities. Her preferred locations for employment include Isère, South-East Lyonnais, or the South-East of France and Switzerland, with a particular interest in opportunities that offer partial remote work.