Regulatory Affairs Associate
CK Group are recruiting for a Regulatory Affairs Associate to join a pharmaceutical company at their site based in Hertfordshire on a contract basis.
The Role: The main purpose of the role will be to
- Administrate the Company’s Medical Device Files and ensure a periodic review of relevant documents
- Administer CAPA investigations, deviations and QA change control process
- Policy and compliance monitoring and support, in line with policies such as social media
Further responsibilities will include:
- Coordinating and managing of approval documents (non-product related) aligned to company standard operating procedures
- Competitor activity tracking and brand scanning via social media and digital channels
- Assisting with compilation of Quality Management report
Your Background: To succeed in this role, you will come from a Life Science background
- Confident in interpreting and communicating scientific data
- Good time management and prioritisation skills
- Excellent communication skills (both spoken and written)
Entitlement to work in the UK is essential. For more information or to apply for this position, please contact Hendre Moolman on 01438 842 970 or email hmoolman@ckgroup.co.uk. Please quote reference 52021.