Senior Regulatory Affairs Associate - Cmc Biologics Vaccines

**When our values align, there's no limit to what we can achieve.**   At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Are you an experienced regulatory affairs professional looking for a new opportunity? We are currently seeking a talented **Senior** **Regulatory Affairs Associate** to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations. As the Senior Regulatory Affairs Associate you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological and vaccines products. **Primary Tasks & Responsibilities:** * Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports. * Assess change controls and provide regulatory assessments of quality changes in production and quality control. * Review study reports from the quality control and production departments to ensure compliance with regulatory requirements. * Coordinate submission preparation with various departments including manufacturing, supply chain, quality control and quality assurance, and other regulatory departments and local companies. * Write and/or review submission content to ensure alignment with regulatory requirements, specifically related to variations and questions from health authorities. * Manage projects within all Regulatory Information Management systems, ensuring the maintenance of worldwide submissions. * Identify, escalate, and mitigate risks associated with regulatory procedures and activities. **Experience and Knowledge Requirements:** * University-level education, preferably in Life Sciences, or equivalent by experience. * Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry. * Strong understanding of CMC and post-approval regulatory requirements. * Experience in writing CMC (technical) sections of regulatory documents such as registration files or variations. * Knowledge of biological or vaccines processes. * Background in validation/Quality Assurance/production in the pharmaceutical industry, with experience in preparing regulatory documentation. Understanding of qualification/validation principles. * Proficiency in Word, PowerPoint, Excel, and experience with Veeva Vault is valued. * Team spirit, flexibility, accountability, and organizational skills. * Fluent in English (written and spoken).