Senior CMC Dossier Writer

7 days ago


Hull, Kingston upon Hull, United Kingdom SRG Full time
Job Title: Dossier Development Scientific Writer

We are seeking an analytical chemist with experience working with Module 3 CMC Dossiers to join our dossier team on a 6-month initial contract to support critical projects.

Key Responsibilities:
  • Support the creation and maintenance of chemistry, manufacturing, and controls information in Module 3 dossiers.
  • Participate in Module 3 strategy and planning meetings, risk assessments, and stakeholder interactions.
  • Write and review regulatory submission documents and prepare responses to questions raised by Healthcare Authorities.
  • Support CMC changes in response to Regulatory Intelligence.
  • Support CMC aspects of Change Control for existing Licenses.
Requirements:
  • Degree or equivalent in a life science subject.
  • Previous experience working with Module 3 Dossiers.
  • Solid understanding of analytical chemistry.

This is a great opportunity to gain experience within CMC regulatory writing and could open the door to Regulatory Affairs positions.

SRG is a global specialty pharmaceutical company dedicated to transforming addiction from a global human crisis to a recognized and treated chronic disease.



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