Associate Director Regulatory Policy

What you’ll bring to the role:  Minimum 8 years of experience in regulatory affairs, drug development or policy development. Health Authority experience is an asset.
Demonstrable history of success over multiple years in a regulatory or health policy role with a strong understanding of the regulatory and legislative environment.
Command of the drug development process, pharmaceutical business, and its regulation.
Organizational awareness (e.g., interrelationship of departments, business priorities), including experience working cross functionally and in global teams.

Please note:

This is a temporary fixed term role of 1 year to provide coverage during a period of employee absence.
We also provide flexible working, learning and development opportunities.
Why Sandoz?  Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic humanrightof good health.
With investments in new development capabilities, production sites, new acquisitions, and partnerships, wehave the opportunity toshape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported!
Join us, help us make healthcare fairer and faster.
Commitment to Diversity & Inclusion:  We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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