Product Life Group - United States

Service Line Lead – NAM Regulatory Development & Sciences at ProductLife Group. Drive end-to-end performance and growth of Regulatory Affairs in North America. Requires 20+ years of regulatory experience in pharma/biotech, a scientific degree, and expertise in global regulatory strategy and Healt...

Senior Director/Principal Consultant (Regulatory Strategy) sought by ProductLife Group to lead U.S. and Health Canada regulatory programs. Requires 15+ years in biotech/pharma regulatory affairs, deep Health Canada expertise, and hands-on FDA/Health Authority interaction. Drive strategy from earl...

Lead U.S. regulatory strategy for biotech and pharma clients at ProductLife Group. This senior consultant role requires 10-15 years' FDA experience, expertise in INDs/NDAs/BLAs, and direct Health Authority interaction. Provide strategic leadership and act as a trusted advisor in this client-facin...

Lead global regulatory submissions for a top consulting firm. Manage end-to-end eCTD publishing using DocuBridge/EXTEDO, ensuring compliance for NDAs, BLAs, and life-cycle filings. This hands-on expert role requires 8+ years' experience and offers leadership of a publishing team.

Launch your career as a VAF 422 Consultant supporting clinical trial systems. This entry-level role requires 0-2 years in BSI and 2-3 years in life sciences, focusing on CTMS configuration, testing, and user support. You will apply ICH-GCP knowledge and assist with system documentation for client...

Seeking a Digital Consultant with a background in pharma, microbiology, or IT. You will configure and support LabVantage LIMS, ensuring compliance with GxP and FDA regulations. This role involves system testing, user support, and data migration for US-based life sciences clients. Prior lab proces...