Regulatory Affairs CMC Associate Contract

Regulatory Affairs Associate CMC, contract jobYour new companyThis 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 roleThe 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 renewalsWhat you'll need to succeedIn 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 returnFlexible working options are available. Hybrid working What you need to do nowFor more information on this or any other Regulatory Affairs contract jobs, please apply to this advert