Regulatory Affairs Specialist

3 weeks ago


Gurgaon, Haryana, India Takeda Full time

Job Summary

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Takeda. As a key member of our Regulatory Affairs department, you will be responsible for leading and developing regulatory strategies for new products, existing products, and pipeline molecules across various regions.

Key Responsibilities

  • Develop and implement regulatory strategies to ensure compliance with local and global regulations
  • Lead cross-functional teams to ensure timely submission of regulatory dossiers and approvals
  • Collaborate with internal stakeholders to ensure alignment with business plans and strategies
  • Stay up-to-date with changes in local and global regulations and communicate effectively with key stakeholders

Requirements

  • Bachelor's degree in Pharmacy or Masters in Chemistry, Sciences, Biotechnology, Biomedical Engineering, Microbiology, or equivalent degree
  • 8-10 years of experience in Pharmaceutical, Medical Device, CRO industry
  • Strong knowledge of local regulations and regulatory corporate policies
  • Excellent verbal and written communication skills
  • Project management and stakeholder management skills

What We Offer

  • A dynamic and supportive work environment
  • Opportunities for professional growth and development
  • A competitive salary and benefits package

How to Apply

If you are a motivated and experienced Regulatory Affairs professional looking for a new challenge, please submit your application.



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