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We are seeking a highly collaborativeRegulatory Affairs Consultant – Compliance & Processto strengthen global regulatory compliance and quality operations across GxP environments. You will partner with Regulatory Affairs, Quality, CMC, Clinical Operations, and other cross-functional teams to enable compliant, efficient, and scalable business operations.
This is a client dedicated project and can be based remotely of from one of our offices.
Key Responsibilities
Controlled Document Management & Governance
Serve as SME for controlled document management, ensuring compliant governance and inspection readiness
Author, review, approve, and manage controlled procedures and quality documents per GxP requirements
Drive document lifecycle management activities including creation, revision, periodic review, and archival