Regulatory Compliance Specialist II

Expert In Recruitment Solutions • Cambridge, Massachusetts, United States • Posted May 16, 2026

Position Overview

Bachelor's required (Master's OK), 2–6 years experience in Pharma / Biopharma Regulatory compliance and manufacturing,

  • Knowledge of GMP. Must have experience in Veeva Vault RIM - work within RSO, ensuring data alignment, submissions, approvals, and license compliance.

  • Strong authoring (GMP, CMC docs, Health Authority responses).

  • UAT experience is a plus (light involvement, not validation-heavy).

  • Must be able to manage multiple priorities, strong communication, works well cross-functionally & independently.






  • The RSO Specialist will work closely with the Manufacturing and Supply teams, and Regulatory CMC colleagues on Vaccines projects. The main focus of this position will be to support a Veeva Vault Rim project requiring previous regulatory and Veeva Vault experience. The RSO specia...