Regulatory Affairs Consultant.8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute to the planning, preparation (including authoring where relevant) and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and/or regional perspective.Working knowledge of EU/US regulatory procedures including post approval requirements. Knowledge of ROW markets regulatory legislations would be an added advantageExperience in handling CMC related health authority queriesGood understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global pharmaceutical legislation and guidance specifically linked to regulatory CMC aspects in the ICH countries.Liaise closely with cross-functional members with aligned product responsibilities.Develop, execute and maintain submission delivery plans, submission content plans, and proactively provide status updates to designated stakeholders.To prepare, review and submit safety variations to Health Authorities and also perform post Approval CMC related updates (where applicable).Prior working experience in Regulatory Information Management Systems like Veeva Vault would be desirable.Strong communications skillsAbility to work independentlyPlease use the below link for job application and quicker response.https://lifelancer.com/jobs/view/4446c2fd328cfbb531a091a9ae0b45d3