Global Regulatory Lead Specialist

hace 5 días


Buenos Aires, Buenos Aires C.F., Argentina Takeda A tiempo completo

Job Summary

We are seeking a highly skilled Global Regulatory Lead Specialist to join our team at Takeda. As a key member of our regulatory affairs department, you will play a vital role in driving regulatory success and ensuring compliance with applicable requirements.

Your primary responsibilities will include:

  • Developing and implementing area regulatory strategies to achieve timely and efficient conduct of development and/or life-cycle management of assigned programs
  • Collaborating with cross-functional stakeholders, including Global Product Teams and Global Regulatory Teams, to ensure effective communication and alignment
  • Evaluating new business development opportunities and participating in due diligence teams as needed

Requirements

To succeed in this role, you will need:

  • A minimum of 8 years of experience in drug regulatory affairs, preferably within the EU/GEM region
  • An advanced scientific-related degree (BSc or BA accepted based on experience)
  • Excellent communication and interpersonal skills, with fluency in English and other local languages
  • Ability to work in flexible hours and prioritize tasks effectively

Working with Us

Takeda is a forward-thinking organization dedicated to delivering innovative solutions that transform the lives of patients. Our team is passionate about creating a positive impact, and we're excited to welcome like-minded professionals to our community.



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