Regulatory Affairs Specialist IIIREMOTE considered. Possibility of extension.Candidate to author/review/approve CMC technical documents in ***'s internal document system to support regulatory submissions (may include BLA, MAA, IND, supplements) to US FDA and international Health Authorities. Must have working knowledge of biologic/drug regulations (FDA, ICH, EU, etc) related to CMC.
Provide regulatory guidance for development projects, post-approval CMC changes/variations. Must have working knowledge of GMPs. Must be well-organized, work with minimal management and meet aggressive timelines.
Utilizes knowledge of word processing software, strong writing and analytical skills to document software capabilities and functionality. This position is working in the CMC area. Relevant experience is required.Experience with drug/biologics licensurePrior regulatory experienceTechnical writing experience (CMC experience)Scientific backgroundCMC/ Regulatory writing experience - 3 + years authoring CMC regulatory documents including Module 2 and Module 2.3Scientific background, vaccines preferredMicrosoft Office (word, excel, powerpoint)Documentum/ Veeva ApplicationsTrackwise ApplicationsICH GuidelinesGMP experienceExperience with drug/biologics licensure preferredPrior regulatory experience