Head of Regulatory

Head of Regulatory page is loaded Head of Regulatorylocations: South Africatime type: Full timeposted on: Posted Todaytime left to apply: End Date: March 16, 2026 (9 days left to apply)job requisition id: 17At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The PositionAs Head of Regulatory Affairs, you will play a pivotal role in ensuring Roche's medicines are registered and compliant with current regulations, enabling the organization to operate optimally while maintaining its license to operate. You will lead the development of regulatory strategies, manage compliance, oversee stakeholder engagement, and contribute to Roche's broader business objectives, always putting the patient first and following the science. Key Challenges Strategic leadership in regulatory affairs, balancing market trends with compliance requirements, and contributing to Roche's long-term organizational ambitions. Developing and implementing policies aligned with legislation, addressing non-compliance and evolving regulatory requirements. Managing relationships with regulatory bodies, industry experts, and external stakeholders while providing guidance to cross-functional Roche teams. Overseeing dossier submissions to ensure timely registration in compliance with national and international standards. Team leadership, including building a talent pipeline, nurturing growth, and developing staff in line with a culture of learning and innovation. Who You Are as Our Ideal Candidate You have a strong entrepreneurial spirit, embracing both compliance and innovation to drive success. As an inclusive leader, you foster trust, inspire teams, and actively contribute to Roche's reputation. You are proactive, self-managed, and able to act boldly, swiftly, and collaboratively, never losing sight of the patient-centric mission.Your qualifications and experience include: A relevant degree (NQF 7/8) in pharmaceuticals with extensive experience (7-10 years in regulatory affairs and 5-8 years in management). Deep knowledge of pharmaceutical regulations, registration processes, and compliance frameworks. A growth mindset, dedication to quality, and the ability to lead under pressure while managing complexity. Exceptional skills in communication, strategic agility, influencing, teamwork, and innovation.Apply today and contribute to Roche's vision of bringing impactful solutions to patients worldwide!Note that relocation benefits are not available for this role. Who we areA healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.Let's build a healthier future, together. Roche is an Equal Opportunity Employer.