Nemera
The Regulatory Affairs Manager leads regulatory and compliance activities for a diverse portfolio of medical devices and combination products, covering various regulatory pathways and risk profiles. The role involves managing the regulatory team, developing regulatory strategies, and ensuring compliance with standards such as MDR 2017/745 and ISO 13485. The position requires close collaboration with internal teams, customers, and external stakeholders throughout the product lifecycle.
Headquarters
Lyon, Auvergne-Rhône-Alpes, France
Company Size
1001-5000 employees
Founded
2015
Nemera is a global drug‑delivery device company that partners with pharmaceutical and biotech firms to develop patient‑centric combination products and delivery solutions. They offer end‑to‑end capabilities — from human‑centered design and engineering through development, regulatory support and scalable manufacturing — to help customers accelerate the sprint to market. Nemera emphasizes putting patients first through ergonomic, compliant devices and integrated services across a range of delivery platforms.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Nemera.
Nemera didn’t post a salary, so this is our estimate from similar listings.
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