Full time

Regulatory Affairs Consultant - CMC biologics (home or office based)

Posted by Parexel • remote, italy, remote, italy, Italy

📍 remote, italy, remote, italy 🕒 February 20, 2026

About the Role

When our values align, there's no limit to what we can achieve.
 

Are you an experienced regulatory affairs professional looking for a new opportunity? We are currently seeking a talented Regulatory Affairs Consultant to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations.

As the Regulatory Affairs Consultant you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.

Primary Tasks & Responsibilities:

  • Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports.

  • Assess change controls and provide regulatory assessments of quality changes in production and quality control.

  • Review study reports from the quality control a...

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