3 days ago Be among the first 25 applicantsDirect message the job poster from Ashford GrayThis is a great opportunity to join a pharmaceutical group which is enjoying significant growth both in Ireland/UK and internationally. The group of companies are proud of its expanding business which includes market leading brands across OTC and Prescription medicines. This role will suit someone who is fast paced and looking to work in a dynamic environment. The company works with a trusted network of global partners to identify and introduce clinically proven products.About the RoleThis role will involve developing and implementing regulatory strategies to support product development and lifecycle management.ResponsibilitiesDevelop and implement regulatory strategies to support product development and lifecycle managementManage a team of Regulatory Affairs Officers to ensure the Company’s products comply with all relevant regulations and standardsEfficiently integrate all new portfolio acquisitions in multiple marketsLead projects on identifying any gaps in dossiers and devising plan to resolve these gapsLead meetings with Regulatory AuthoritiesLead regulatory aspects of internationalising products and applying for reclassification of productsMonitor and interpret regulatory trends and changes relevant to the industry and pro-actively keep the Company appraised of theseCollaborate cross functionally with Quality and Commercial/Marketing teams to achieve Company objectivesQualificationsMinimum of 8-10 years previous experience will be neededRequired SkillsHighly resilient and adaptable, able to work under pressure and within time constraintsDrives results on a timely basis and sees things through to conclusionStrong knowledge of global regulatory frameworksKnowledge of MRP, DCP, CPKnowledge of medical devices highly desirableExcellent attention to detail and organisational skillsCapable of working on own initiative and taking responsibility for course of actionFlexible and fast pacedPay range and compensation packageEqual Opportunity StatementThe company is committed to diversity and inclusivity.```Seniority levelSeniority levelExecutiveEmployment typeEmployment typeFull-timeJob functionJob functionQuality Assurance and ManufacturingIndustriesPharmaceutical Manufacturing and Medical Equipment ManufacturingReferrals increase your chances of interviewing at Ashford Gray by 2xSign in to set job alerts for “Regulatory Affairs Manager” roles.Senior Regulatory Affairs Specialist - PharmaRegulatory Affairs Manager - PharmaceuticalsWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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