Global Site CMC Regulatory Director (Post-Approval)

A global biopharmaceutical firm is seeking a Director Regulatory Site CMC in Cambridge, Massachusetts to lead post-approval change management activities and ensure compliance with global requirements. The ideal candidate will have over 10 years in the industry, including 8 years in Regulatory CMC, and will be proficient in communicating regulatory strategies. This role offers a hybrid working model and the opportunity to drive standardization and automation in regulatory processes.
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