Regulatory Affairs Associate Director, CMC

We are looking for a Regulatory Affairs Associate Director, CMC to contribute to the development and delivery of global Chemistry, Manufacturing and Controls (CMC) regulatory strategies across a portfolio of products.

In this role, you will support regulatory activities across development and lifecycle stages, ensuring high-quality submission content and alignment with global regulatory requirements. Working closely with cross-functional partners, you will help enable timely approvals and maintain compliant, consistent product information across markets.

Major Accountabilities

• Contribute to the development and implementation of global CMC regulatory strategies for assigned projects and products.
• Plan, coordinate, and support CMC submission activities, including authoring, review, and submission of documentation.
• Identify documentation requirements and manage alignment on content, quality, and timelines across stakeholders.
• Author and review high-quality CMC regulatory documentation, ensuring compliance with applicable guidelines and standards.
• Communicate regulatory considerations, risks, and updates to cross-functional project teams and stakeholders.
• Contribute to and support Health Authority interactions, including preparation of briefing materials and responses.
• Collaborate across functions to support consistent delivery and alignment on regulatory activities.
• Contribute to continuous improvement initiatives and support knowledge sharing within the regulatory community.

Essential Requirements

• Fluency in English (written and spoken).
• Degree in a scientific discipline (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent experience.
• Demonstrated capability in CMC Regulatory Affairs, including regulatory submission and approval processes.
• Strong understanding of CMC regulatory requirements, with the ability to navigate complex regulatory topics and contribute to regulatory strategy.
• Ability to evaluate scientific data across multiple disciplines and translate insights into regulatory decision-making and documentation.
• Working knowledge of pharmaceutical development, manufacturing, or related scientific areas.
• Ability to collaborate effectively and influence within cross-functional, global matrix teams while managing multiple priorities.
• Strong planning, organisational, and interpersonal skills, with a focus on quality, delivery, and continuous improvement.

Commitment to Diversity and Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.