Regulatory Affairs Associate (CPT/OPT)

Company DescriptionKatalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.Job DescriptionCompany Description:Katalyst HealthCares & Life Sciences Inc., is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.We are an E-Verified company, looking for prospective candidates on OPT and CPT and we also provide H1B (CAP and CAP exempt) and Green Card sponsorship's as well for eligible candidates.We have a few immediate job opportunities available in Regulatory Affairs Operations, CMC, Publishing and Submission for Clinical and Non-Clinical areas. We work with University hospitals, pharmaceutical companies and recruiting partners.Responsibilities:This position will assist with the preparation and submission of ANDAs, Amendments, Supplements and Annual Reports to appropriate regulatory agencies.This position will also provide support of the regulatory function through document management, electronic submission compilation and management, and other group management activities as required. Works with Regulatory Affairs, Quality Assurance, Quality Control, Manufacturing, Research and Development groups, Information Technology, and other departments as needed.May submit submissions for changes to labeling, QC, manufacturing, or distribution practices. Keeps abreast of regulatory compliance issues and assist in developing new Regulatory Department procedures, as needed.Responsibilities Prepare, assemble, review and/or evaluate, publish and archive new ANDA and life cycle management regulatory submissions in accordance with local regulatory requirements and guidelines. Prepare paper based and electronic submissions, including both eCTD and non-eCTD formats, for multiple project to regulatory agencies, and ensure the timely delivery of quality submissions.Critically review submission documentation and provide input to respective departments for necessary revisions.Coordinate and prepare responses to FDA Deficiency Letters and other agency requests.Using eCTDXpress complete submission publishing for submission through ESG.Qualifications:BS or MS in scientific discipline or equivalent education and experience.Minimum 1-3 years previous work experience in the pharmaceutical industry, preferably in the area of drug regulatory affairs, analytical, QA, R&D or production experience.Must have a working knowledge of US Regulatory Operations and Submissions.Additional InformationAll your information will be kept confidential according to EEO guidelines.