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Displaying 1-1 of 1 of the latest remote CTD regulatory affairs jobs

  • Syner-G BioPharma Group 🧬🧪🔬

    16 days ago

    Senior Regulatory Affairs Specialist, CMC

    The Senior Regulatory Affairs Specialist, CMC is responsible for providing regulatory CMC support through the product life cycle, including regulatory strategies, submission timeline development, change control, and preparing submission documents. The role involves authoring and reviewing CMC regulatory documents, assessing CMC changes, and ensuring compliance with regulations.

    Syner-G BioPharma Group and Sequoia Biotech Consulting merged in September 2024, uniting two industry leaders to create a new force in life sciences consulting.

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1 Based on analysis of over 1,200 job applications.