Netty Manette

Netty Manette

Responsable Qualité Système Et Digitalisation @ Berry

About Netty Manette

Netty Manette is a quality system and digitalization manager at Berry Global, Inc., with extensive experience in quality assurance and regulatory affairs in the pharmaceutical industry. She has held various roles at Valdepharm and Sanofi Pasteur, and she holds two master's degrees in organic chemistry and product development in health.

Work at Berry Global

Netty Manette has been employed at Berry Global, Inc. since 2022, serving as Responsable qualité système et digitalisation. In this role, she oversees quality system management and digitalization initiatives, contributing to the company's commitment to maintaining high standards in product quality and operational efficiency.

Current Role at Valdepharm

In addition to her position at Berry Global, Netty Manette has worked at Valdepharm since 2018 as Responsable assurance qualité opérationnelle. Her responsibilities include ensuring operational quality assurance processes are adhered to, which is critical for maintaining compliance and product integrity within the pharmaceutical sector.

Previous Experience in Regulatory Affairs

Netty Manette has a background in regulatory affairs, having worked at Sanofi Pasteur with Umanis as Chargé d’affaires réglementaires from 2015 to 2016. She also held the position of Chargé d’affaires réglementaires at Valdepharm from 2016 to 2017, where she focused on regulatory compliance and product development processes.

Educational Background

Netty Manette holds a Master in chimie organique from Université Paris-Sud, which she completed in 2013. Additionally, she earned a Master en développement de produit de santé from Université de Limoges in 2014. Her education has provided her with a strong foundation in organic chemistry and health product development.

Career Progression at Valdepharm

Netty Manette has had a significant career at Valdepharm, where she served as Responsable compliance from 2017 to 2018. This role involved ensuring that the company's operations met regulatory standards, further enhancing her expertise in quality assurance and compliance within the pharmaceutical industry.

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