Regulatory Affairs Manager
hace 3 semanas
Job Description:
">- Manage global regulatory submission projects and contribute to the technical regulatory strategy for developing and registering products worldwide.
- Collaborate with internal teams and external contacts to implement global systems, tools, and processes supporting product development and market expansion.
- Represent Novartis on specific projects and ensure adherence to company policies and guidelines.
- Analyze data, prepare reports, and communicate insights to stakeholders.
About the Role:
As a key member of our team, you will play a crucial role in ensuring compliance with regulatory requirements and driving business growth through effective strategic planning and project execution.
Key Responsibilities:
• Manage medium to small-scale global regulatory submission projects
• Contribute to the development of technical regulatory strategies for new and existing products
• Collaborate with cross-functional teams to implement global systems and processes
• Ensure adherence to Novartis policies and guidelines
• Analyze data and prepare reports to inform decision-making
Requirements:
• Bachelor's degree in a relevant field (e.g., life sciences, law)
• 5+ years of experience in regulatory affairs or a related field
• Strong understanding of regulatory requirements and industry trends
• Excellent communication and project management skills
• Ability to work in a fast-paced environment and prioritize multiple tasks
What We Offer:
• Competitive salary: $120,000 - $160,000 per year
• Comprehensive benefits package, including health insurance, retirement plan, and paid time off
• Opportunities for professional growth and development
• Collaborative and dynamic work environment
• Recognition and rewards for outstanding performance
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