Senior Director, Regulatory Affairs
Abata TherapeuticsFull Time
Expert & Leadership (9+ years)
Paris, Île-de-France, France
Key technologies and capabilities for this role
Common questions about this position
This is a fully remote position as Veeva is a Work Anywhere company, supporting flexibility to work from home or in the office.
This information is not specified in the job description.
Candidates need at least 10 years of significant management and R&D consulting experience, expertise in Life Sciences particularly Regulatory Affairs and Regulatory Information Management, an extensive network in Top 20 Life Sciences companies, and a proven track record in developing high-value customer engagements and digital transformation programs.
Veeva's core values are Do the Right Thing, Customer Success, Employee Success, and Speed.
A strong candidate will have 10+ years in R&D consulting, deep Life Sciences experience in Regulatory Affairs, an established network with Top 20 Life Sciences leaders, and proven success in business development and digital transformation projects.
Quality and regulatory software solutions provider
Veeva Systems offers software solutions for quality, regulatory, and advertising claims management, focusing on consumer products and chemical companies. Their cloud-based platform provides visibility and traceability throughout the product journey, ensuring compliance with regulations and accelerating time-to-market. Unlike competitors, Veeva has specialized expertise in both the Life Sciences and Chemical sectors, allowing them to effectively address industry-specific challenges. The company's goal is to help clients efficiently bring safe and compliant products to market.