Regulatory Affairs Senior Associate
6 month contract
Liverpool based - Hybrid working with 3 days onsite
Offering up to £40.00 Per Hour via PAYE
Strong potential for extension
CPL Life Sciences is collaborating with a leading pharmaceutical firm, whose core focus is the continued development of the influenza vaccine. Our client is looking for a Senior Regulatory Affairs Associate within CMC initially on a 6 month contract to be based from their Liverpool site. Working within the CMC and Compliance team, you will be contributing to the implementation of global and regional objectives by leading and executing the CMC strategy for multiple products.
Core Responsibilities include;
- Lead and assist in the development and implementation of the global CMC regulatory strategy
- Lead the authoring, preparing and compiling of high quality, submission-ready CMC documentation for HA submissions
- Ensure compliance of CMC regulatory dossiers with manufacturing and quality control processes
- Support global CMC regulatory and change control policies and procedures
Candidate Requirements include;
- Eligibility to live and work in the United Kingdom
- A Life Sciences degree or equivalent
- Up to 2 years experience within Regulatory experience
- Able to work on site 3 days per week
-Experience working in a CMC environment is advantageous not a requirement
- Prior experience supporting UK and EU Affiliates is a benefit
- Able to work on site 3 days per week
If this opportunity is of interest to yourself please forward your up to date CV to Sophie.Malyon@cpl.com.
- Agency: Cpl Life Sciences
- Reference: JO-2302-509829
Website: Cpl Life Sciences
- Posted: 10th March 2023
- Expires: 7th April 2023
