Director, Regulatory Affairs Lead

3 weeks ago


Hyderabad, Telangana, India Bristol Myers Squibb Full time

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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