Operating at the intersection of science, policy, and strategy, this role drives the proactive monitoring, interpretation, and influence of global cGMP regulations and guidelines, translating insights into impactful Quality Standards (policies and procedures) that support breakthrough therapies. * Act as a senior industry representative in global regulatory forums, trade associations, and health authority engagements (e.g., EFPIA, EMA, MHRA, ICH, etc.), shaping emerging regulations and advocating for science- and risk-based approaches aligned with Pfizer's strategic priorities.
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