Opportunity for Director Regulatory Affairs @ AstraZeneca


Website AstraZeneca

About AstraZeneca

AstraZeneca makes a substantial contribution to the United Kingdom that extends beyond the mere supply of our medications and the advantages they bring to the nation’s health. In 2009, we took the initiative to commission a comprehensive report aimed at quantifying our noteworthy economic impact on the UK. This impact encompasses not only our investments in jobs but also the generation of wealth. To ensure objectivity and accuracy in this analysis, we engaged the services of Oxera, a reputable independent economic consultancy. Their expertise aided us in assessing and understanding the full scope of our contributions to the UK economy.

Post: Director Regulatory Affairs, Late Cardiovascular, Renal and Metabolism

Job Description

Impactful Role in Changing Patients’ Lives

Join AstraZeneca as a Regulatory Affairs Professional and make a difference by leveraging our scientific expertise to improve patients’ lives. In this crucial role, you’ll shape the trajectory of our innovative pipeline, craft regulatory strategies for therapeutic assets, and engage Health Authorities to guide our development initiatives. Through your efforts, our Regulatory Affairs teams convert groundbreaking science into vital medications for global patients.

Strategic Leadership for Complex Impact

As you progress in experience, your accountability for strategic leadership grows. You’ll spearhead the development and execution of global regulatory strategies for increasingly intricate product portfolios. Your regulatory proficiency must align with strategic thinking, innovative prowess, persuasive influencing, and effective communication. Embrace novel regulatory tools and foster a culture of shared learning, ensuring our medicines benefit from the latest regulatory advancements. Speak the regulatory voice across all organizational levels with confidence.

Qualifications and Expertise Required at AstraZeneca

  • Hold an academic degree in a science-related field or its equivalent
  • Possess extensive knowledge of regulatory affairs across one or more therapeutic domains in both early and late development
  • Showcase a proven track record in regulatory drug development, encompassing product approval and launch
  • Demonstrate experience in leading interactions with Major Health Authorities
  • Exhibit the capacity for strategic and critical thinking, including risk assessment for regulatory activities
  • Thrive in strategically navigating complex, business-critical, and high-profile development programs

Additional Information

  • Location: Bangalore
  • Industry Type: Pharma
  • Functional Area: Regulatory Affairs
  • End Date: 10th September 2023
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To apply for this job please visit astrazeneca.wd3.myworkdayjobs.com.