Director, Regulatory Affairs Lead
3 weeks ago
Job Summary
Seeking a seasoned Regulatory Affairs Leader to oversee the GSRD team in Hyderabad, ensuring seamless regulatory documentation processes and compliance with global standards.
About the Role
This is a unique opportunity to leverage your leadership skills, scientific expertise, and passion for regulatory affairs to drive business growth and excellence at Bristol Myers Squibb. As a key member of our team, you will be responsible for implementing regulatory documentation standards, managing project timelines, and fostering a culture of collaboration and innovation.
Key Responsibilities
- Lead the GSRD team in Hyderabad, providing strategic guidance and technical support to ensure regulatory compliance and quality documentation.
- Develop and implement regulatory documentation standards, processes, and procedures to support global submissions and business objectives.
- Collaborate with cross-functional teams to ensure alignment with business needs, objectives, and regulatory requirements.
- Provide technical expertise and support to colleagues, ensuring high-quality regulatory documentation and compliance.
- Stay up-to-date with global regulatory developments, trends, and best practices, applying this knowledge to drive business excellence.
Requirements
To be successful in this role, you will need:
- Prior experience in regulatory affairs, preferably in the pharmaceutical industry, with a strong understanding of regulatory documentation processes and standards.
- Proven leadership skills, with the ability to manage complex projects, teams, and stakeholders.
- Excellent communication, interpersonal, and collaboration skills, with the ability to build strong relationships with colleagues, partners, and external stakeholders.
- A strong understanding of global regulatory requirements, trends, and best practices.
- Ability to work in a fast-paced environment, prioritizing tasks, managing multiple projects, and meeting deadlines.
What We Offer
Bristol Myers Squibb is a global leader in the pharmaceutical industry, dedicated to transforming patients' lives through science. We offer a competitive compensation package, comprehensive benefits, and opportunities for professional growth and development. If you are a motivated, results-driven professional with a passion for regulatory affairs, we encourage you to apply for this exciting opportunity.
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