Director, Governance & Cross-functional Lead, Regulatory Affairs Advanced Synthesis (f/m/d)

Director, Governance & Cross-functional Lead, Regulatory Affairs Advanced Synthesis (f/m/d)

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

As Director, Governance & Cross-functional Lead – Regulatory Affairs (RA) within our Advanced Synthesis Platform you will be leading a team within a matrix structure (cross-functional, cross-technological and regional coordination). This Team Lead position is a high-impact role focused on shaping the overall regulatory strategy and supporting business growth initiatives and serving as a key connector across global, regional, and technology teams to ensure a scalable, adaptable, and business-aligned regulatory framework.

Key responsibilities:

• Manage a team within a hybrid matrix setup that supports multiple sites and technologies.
• Act as a regulatory liaison between local teams and regional/global regulatory leadership and collaborate with Regional Regulatory Experts and Leads to implement harmonized regulatory strategies across all locations.
• Lead regulatory input for new business opportunities, mergers, acquisitions, and site expansions.
• Act as the primary regulatory interface for Growth Project Teams, ensuring compliance considerations are integrated early
• Align closely with the Global Regulatory Affairs Lead for Advanced Synthesis as well as with RA leads from other sites to create a scalable regulatory Affairs framework that can flex with business demands.
• Drive process efficiencies that improve speed-to-market while maintaining compliance and support urgent projects and regulatory filings to keep pace with market opportunities.
• Communicate with peer Local Leads at other sites to share best practices, resolve challenges, and improve adaptability and provide regulatory guidance to site leadership teams, ensuring alignment with overall business objectives.
• Partner with internal and external stakeholder for preparation (write and/or review ) of high-quality CMC submissions that satisfy the critical regulatory criteria set by FDA, EMA, and/or other significant regulatory bodies, while also aligning with corporate objectives and relevant legislation.
• Proactively oversee the regulatory CMC aspects of programs, providing guidance, managing the preparation, and ensuring the submission of CMC documentation supporting clinical trial applications and marketing submissions, in alignment with the development phase.
• Review and evaluate the regulatory impact of the change requests for Drug Substances and Drug Products manufacturing process incl. technology transfer.
• Prepare and submit country-specific health authority supporting documents such as Drug Master Files (DMFs), Site Master Files (SMF) or other records on behalf of customers.
• Utilize prior analytical (Quality Control, Analytical Development) and/or manufacturing process (Operation) or Quality Assurance or Program Management experience to question and propose alternative solutions to challenges by internal and external customers.
• Monitor emerging regulations, industry trends, and best practices to keep the organization proactive.

Key requirements:

• Degree in Regulatory Affairs, Chemistry, Biology, Biochemistry, Pharmacy or equivalent
• Extensive experience (10 years +) in the pharmaceutical and biotechnology industries, specializing in small and midsize molecules with additional understanding of large molecules.
• Experience in leading small groups and complex programs (team or matrix)
• Experience in leading programs on behalf of internal or external stakeholders
• Exceptional communication and writing skills, fluency in English (additional languages like German are advantageous)
• Proactive, problem-solving attitude, with a deep commitment to regulatory excellence and a passion for driving healthcare innovation.
• Independent, self-motivated, organized, able to multi-task, skilled in communication with capability to excel in a dynamic, cross-functional matrix environment
• Team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

#J-18808-Ljbffr