Regulatory Affairs Manager.

Regulatory Affairs ManagerIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.Job DescriptionPrimary Role: Under the general direction of the CMC Regulatory Affairs team, develop a Core Dossier for Module 2.3 and Module 3 CTD sections for a marketed product, and leverage the Core Dossier documents to support Marketing Authorization Applications for international regions. Manage preparation of Core Dossier and CMC components for international marketing applications in a timely manner to meet corporate objectives. Responsibilities:50% of the time develops global CMC Core Dossier for Module 2.3 and Module 3 CTD sections50% of the time prepares CMC components of new Marketing Authorization Applications for international countriesSomeone who can review the current NDA.QualificationsRequirements :Bachelor's degree in pharmacy, biochemistry, chemistry, biology or related pharmaceutical field. (Pharma/Biotech is a Must Have)Need 5-8 years of experience with Global Submissions (US and European Knowledge) requiredActively involved in writing or reviewing applications to understand what content is required.Must have Regulatory CMC Experience (5-8 years).Must have knowledge of BLA or NDA.Cannot come directly from Education.Know content module 2-3 for CMC.Key Skills and Competencies:Knowledgeable in ICH guidelines, Latin American CMC and core dossier requirementEnsures timely delivery of high quality regulatory submissionsMust be highly organized, committed to excellence, and possess both determination and attention to detail.