Steven Jones

About Steven Jones

Accomplished Regulatory Affairs and Product Development Executive with over 25 years of experience leading innovation and compliance across the pharmaceutical, biotechnology, and animal health industries. I specialize in Chemistry, Manufacturing, and Controls (CMC), regulatory strategy, and global dossier management — with a strong track record of guiding products from concept through approval and market launch.My career has been defined by driving cross-functional collaboration, accelerating development timelines, and ensuring regulatory alignment across diverse markets including the US, Canada, EDQM, and ROW. I’ve led teams through complex product development cycles, authored regulatory submissions for APIs and drug products, and engaged directly with global health authorities to secure approvals and maintain compliance.With a deep understanding of scientific principles, regulatory frameworks, and operational execution, I bring clarity to complexity — enabling organizations to innovate confidently, reduce risk, and deliver high-quality products to market. I’m passionate about advancing health through strategic leadership, regulatory excellence, and collaborative problem-solving.

Experience

1. Head of Global Regulatory Affairs Cmc, Us

   Boehringer Ingelheim

   Apr 2019 — Present

Skills

• Quality System
• V&V
• Quality Assurance
• Capa
• Gmp
• Validation
• Sop
• Electronic Registrations and Drug Listings
• Fda
• Quality Management
• Microbiology
• R&D
• Spl
• Drug Product
• Biotechnology
• Database Management
• Ectd
• Regulatory Requirements
• Regulatory Affairs
• Regulatory Submissions
• Glp