About the job
About Nūmi
Nūmi is a pioneering bioproduction platform that utilizes human mammary cells to generate essential ingredients with documented health advantages throughout all life stages. Specifically, we are the first European company dedicated to cultivating breast milk, aiming to deliver human milk components that closely align with optimal infant nutrition!
Based in the vibrant center of Paris (Hôpital Cochin, Paris 14th), Nūmi is an early-stage, VC-backed biotech firm, bolstered by esteemed investors and scientific collaborators.
Nūmi's Core Values
- Positivity: We foster a culture of positivity, driven by our mission to communicate with enthusiasm and clarity, while consistently focusing on our larger impact. We acknowledge quick victories but remain steadfast in our long-term objectives.
- Excellence: We believe excellence is rooted in commitment and continuous enhancement. We view challenges as opportunities for growth and strive to deliver superior results through diligence, attention to detail, and integrity, evolving as individuals and a cohesive team.
- Teamwork and Pedagogy: We understand that collaboration strengthens us. Nūmi encourages knowledge-sharing, constructive feedback, and mutual respect among team members, ensuring collective success.
- Ambition: We set high aspirations and encourage bold thinking. Nūmi is propelled by innovative ideas and unwavering resolve, always reaching for significant achievements.
Position Overview
As we delve deeper into regulatory pathways across various jurisdictions, we are in search of a senior leader to oversee quality and regulatory strategies, ensuring that Nūmi’s scientific outputs meet the requisite standards and that our regulatory submissions are executed with accuracy and foresight. This role is critical to Nūmi’s growth and market entry strategy. As we establish a groundbreaking product segment, the development of a robust quality framework and the effective implementation of regulatory strategies are vital to our success. You will convert external regulatory counsel insights into actionable internal quality systems, align cross-functional requirements, and propel dossiers towards submissions in key regions by the conclusion of 2026.
As a strategic leader and quality advocate, you will ensure that regulatory and quality practices are not just compliant but optimized for efficiency, consistency, and innovation.
