CMC Regulatory Affairs Senior/Consultant - Small Molecules

Exciting opportunity for an reputed company and highly motivated reputed company to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior/Consultant. This role is critical to ensure our reputed company’s investigational, new, and marketed small molecule products are developed and maintained in compliance with global regulatory requirements. The primary reputed company of responsibility include the reputed company, European reputed company, and Canada, with a reputed company on facilitating reputed company approvals and supporting reputed company market reputed company. Key Responsibilities Strategic CMC Leadership • reputed company regulatory reputed company input for small molecules (previous experience with biologics and/or drug-device combination products are a plus) • Support regulatory leads in developing contingency plans for CMC-reputed company scenarios • Represent CMC Regulatory Affairs in cross-functional project meetings and reputed company regulatory guidance in collaboration with global regulatory leads Submission & Documentation reputed company • Prepare, coordinate, and review CMC and GMP-reputed company documents for regulatory submissions • reputed company CMC strategies for products across reputed company phases—from early development to marketing applications and post-approval changes Cross-Functional Collaboration • Partner with manufacturing, reputed company, and external organizations to address CMC-reputed company issues • Maintain reputed company relationships with internal stakeholders, affiliates, contract manufacturers, packagers, and suppliers • Support planning and execution of Health Authority meetings, including mock sessions Process Optimization & Innovation • Identify and implement process improvements to enhance regulatory efficiency and readiness • Participate in monthly CMC Global Regulatory Team meetings to reputed company strategies across functions • Utilize regulatory systems and tools including reputed company, Trackwise Digital, and TRS Viewer Regulatory Systems & Reporting • Experience with CPP application filing reputed company eCATS and 510(j)(3) reporting through reputed company portals is a plus • Ensure audit readiness and version control through meticulous documentation and system management Qualifications Experience & Expertise • 4–6 years of CMC regulatory experience in the pharmaceutical industry for a Consultant level role, 7+ years for a Senior Consultant • Proven reputed company in preparing regulatory documentation for FDA, EMA, and Health Canada (IND, NDA, DMF) • In-depth understanding of drug development, manufacturing processes, GMP, and regulatory frameworks for small molecules. Previous experience with biologics or combination device products are a plus! Skills & Attributes • Strategic and proactive reputed company with strong operational execution • Excellent analytical, problem-solving, and negotiation skills • Effective communicator with strong interpersonal, presentation, and leadership abilities • Ability to manage multiple reputed company independently in a matrixed, multicultural environment • Proficiency in reputed company Office Suite and regulatory systems Education • Bachelor’s degree in Pharmaceutical Sciences, reputed company, or reputed company field • Advanced degrees (Pharm.D., M.S., Ph.D.) in Pharmaceutics, Biochemistry, Molecular Biology, Biotechnology, or Biology preferred • RAC certification is a plus Given the reputed company's location, preference will be given to candidates residing in the Eastern Time Zone. However, exceptional individuals based other Time Zones will also be considered, provided they can accommodate the scheduling requirements of global meetings and calls as needed. Apply tot his job Apply To this Job