Regulatory Affairs Associate CMC, contract job
Your new company
This well-known biopharma is looking for an experienced Regulatory Affairs CMC Associate to join their Regulatory Affairs CMC International Team. This is a 12-month contract job with working from home (wfh / hybrid) options.
Your new role
The successful Regulatory Affairs CMC Associate will be responsible for co-ordinating the preparation of high quality CMC documents to support regulatory submissions in International regions, (Asia, Latin America, Middle East, Eastern Europe and Africa) and working with pharmaceutical development, manufacturing, QA and external partners to deliver the CMC components for licence renewals
What you'll need to succeed
In order to be considered for this contract job as Regulatory Affairs CMC Associate, you must have some experience in CMC regulatory affairs and awareness of regulatory requirements, including ICH requirements and regional requirements, and be capable of the preparation and finalisation of CMC regulatory dossiers.
What you'll get in return
Flexible working options are available. Hybrid working
What you need to do now
For more information on this or any other Regulatory Affairs contract jobs, please apply to this advert