Senior Regulatory Affairs Consultant - CMC Biologics

Senior Regulatory Affairs Consultant 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. Senior Regulatory Affairs Consultant- CMC Biologics Extensive experience in managing new registrations, life cycle maintenance, and renewals for biological products including vaccines, recombinant proteins, monoclonal antibodies, and plasma‑derived therapies across major markets such as the US, EU, Japan, Canada, Switzerland and Australia. Contribute to preparation (including authoring where relevant) and delivery of regulatory submissions from a global and regional perspective. Preparation and review of Marketing Authorization Applications & Variations for filing in US, EU, Japan, Canada Switzerland, Australia. Good 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. Strong communication and collaboration skills, ability to work independently. The role is for a team lead with expectations to guide/mentor team members on technical aspects including regulatory filings to global markets Experience level: 10 to 14 years of relevant experience Location: India Remote Education: Minimum of a bachelor’s degree in a Scientific or Technical Discipline, Advanced Degree preferred Experience Level Senior Level