Global Medical Affairs Quality Lead

Drive regulatory quality in Global Medical Affairs with AstraZeneca, focusing on governance, risk assessment, and compliance. Shape quality programs and ensure audit readiness while leading cross-functional initiatives.

As a leader, you will develop and enhance the Global Medical Affairs quality program, aligning regulatory processes with best practices.

Your role involves fostering communication across teams to promote cohesive collaboration and ensure that all functions understand quality management concepts. You'll also guide the development of quality training and manage tools to track key quality metrics.

Key Responsibilities:

• Develop and implement robust quality programs for Global Medical Affairs

• Lead regulatory quality forums and inspection readiness teams

• Identify collaboration opportunities across functions

• Manage tools for tracking quality metrics and compliance

• Communicate effectively at all organizational levels

Requirements:

• 10+ years in pharmaceutical or biopharmaceutical industry

• Minimum 4 years in a quality role or quality systems

• Bachelor's or advanced degree in Life Sciences

• Strong management and problem-solving skills

• Experience with GCP or GVP regulations

Engage in quality management initiatives and demonstrate leadership to enhance AstraZeneca's commitment to regulatory excellence.
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