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Senior CMC Dossier Writer
2 months ago
Job Title: Senior CMC Dossier Writer
Job Type: 6 Month Contract - Potential to Extend
Salary: Competitive and Negotiable
Location: Hybrid - Remote Working Possible
About the Company:
SRG is a global specialty pharmaceutical company dedicated to transforming addiction from a global human crisis to a recognized and treated chronic disease.
About the Role:
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. The successful candidate will support critical projects and gain experience in CMC regulatory writing, potentially opening the door to Regulatory Affairs positions.
Key Responsibilities:
- Support the creation and maintenance of chemistry, manufacturing and controls information in Module 3 dossiers (CTD, IMPD, IND, MAA, NDA, ASMF and DMF) covering drug substance and drug product.
- Participate in Module 3 strategy and planning meetings, risk assessments and stakeholder interactions to leverage technical and regulatory expertise and insight.
- 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 Licences.
Requirements:
- Degree or equivalent in a life science subject.
- Previous experience working with Module 3 Dossiers.
- Solid understanding of analytical chemistry.