Offer summary

Qualifications:

Bachelor's degree in life sciences or related field is required., Experience in regulatory affairs within the pharmaceutical or biotechnology industry is essential., Strong understanding of regulatory guidelines and submission processes is necessary., Excellent communication and project management skills are important..

Key responsibilities:

Oversee the preparation and submission of regulatory documents to health authorities.

Coordinate with cross-functional teams to ensure compliance with regulatory requirements.

Monitor changes in regulations and assess their impact on the organization.

Provide guidance and support to junior regulatory staff and stakeholders.

Founded in 2018, VIVERE is transforming the fast-moving consumer goods (FMCG) industry. Using AI to power our Platform model, we efficiently create and manage next-generation brands. Our integrated model combines marketing, design, R&D, production, supply chain management, sales, and technology. We have successfully launched 10 brands and 150 products in markets such as beauty, health, wellness, pet care, and home & garden. We sell through Amazon, direct-to-consumer (DtC) channels, and retail. We co-develop brands with creators and communities such as Zumba and help other brands develop high-quality products through our B2B services. We are a team of 60 consumer experts based in Hamburg, where our production facility is also located. VIVERE is becoming a key player in Europe, the United States, and the Middle East.

Required profile