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PHARMA JOBS POST > Bangalore > AstraZeneca hiring for Regulatory Affairs Manager I at Bangalore
BangaloreBengaluruHiringRegulatory Affairs

AstraZeneca hiring for Regulatory Affairs Manager I at Bangalore

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Last updated: June 16, 2024 5:12 pm
ADMIN 11 months ago 863 Views
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AstraZeneca hiring for Regulatory Affairs Manager I at Bangalore

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Regulatory Affairs Manager IAPPLY NOW

Regulatory Affairs Manager I

📍India – Bangalore

Job Title: Regulatory Affairs Manager I

Career Level – D

Introduction to role:

The Regulatory Affairs Manager I is a regulatory specialist with project management capabilities responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables, including delivery as an individual contributor, if required. The Regulatory Affairs Manager I is fully proficient in applying established standards to perform regulatory affairs management for simple/moderately complex products/regions and under minimal supervision. Capable of leading cross functional activities. Participates continuous improvement of process and tools/systems.

Accountabilities:

Regulatory Affairs Management contributes to regulatory submission strategy, identifying submission risks and opportunities, while leading simple through more complex regulatory applications and managing procedures through approval. Provides regulatory expertise and guidance on procedural and documentation requirements to GRET, Global Regulatory Strategy Team (GRST) and cross-functional teams working flexibly within and across regions to ensure the delivery of business objectives. Provides regulatory labeling expertise and leads the maintenance of labeling documents for allocated products. Is responsible for the regulatory activities involved in the coordination, development and implementation of revised printed labeling for allocated products and other regional labeling.

Essential Skills/Experience:

– Relevant University Degree in Science or related discipline

– Minimum 6 years of relevant Regulatory experience within the biopharmaceutical industry, including license maintenance, labelling and publishing, and of working in regulated markets

– General knowledge of drug development

– Good knowledge of the regulatory product maintenance process

– Strong project management skills

– Leadership skills, including experience leading multi-disciplinary project teams

Desirable Skills/Experience:

– Excellent English written and verbal communication skills

– Cultural awareness

– Scientific knowledge sufficient to understand regulatory issues and facilitate scientific discussions

– Proficiency with common project management (e.g., MS Project) and document management tools

– Ability to work independently and as part of a team

– Influencing and stakeholder management skills

– Ability to analyze problems and recommend actions

– Continuous Improvement and knowledge sharing focused

– Basic understanding of emerging technologies like AI, ML etc

– Demonstrate ability to use digital tools and solutions relevant to own work tasks to support productivity, collaboration and learning

– Work proactively to understand future needs and opportunities for digital transformation that improve the effectiveness and speed of core business processes and decision making.

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