Regulatory Writer

1 week ago

United Kingdom SRG Full time

Job Title: Dossier Development Scientific Writer
Type: 6 Month temp – Potential to extend
Location: Hull, England, Hybrid – Remote working is possible for the right candidate.


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

As a result of expansion, we are looking for an analytical chemist who has experience working with Module 3 CMC Dossiers to join the dossier team on a 6 month initial contract to support with a range of critical projects. This is a GREAT opportunity to gain experience within CMC regulatory writing, and could open the door to Regulatory Affairs positions.

32P2 Pharmaceutical Development

Actively participate in Module 3 strategy and planning meetings, risk assessments and stakeholder interactions to leverage your technical and regulatory expertise and insight, to drive the right decisions at the right time and mitigate risk.
Write and review regulatory submission documents and prepare responses to questions raised by Healthcare Authorities.
Support CMC changes in response to Regulatory Intelligence.
SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

We’re committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.


If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit to view our other vacancies.

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