Regulatory Affairs Expert

2 days ago


Gurgaon, Haryana, India Lifelancer Full time

Job Title: Regulatory Affairs Expert - Pharmaceutical Product Registration

Overview:

Lifelancer, a talent-hiring platform in Life Sciences, Pharma and IT, seeks an experienced Regulatory Affairs Expert to join our team. As a key member of our regulatory department, you will play a crucial role in ensuring the timely registration of pharmaceutical products with regulatory authorities.

About the Role:

We are seeking a highly motivated and organized individual with a strong background in regulatory affairs. Your primary responsibility will be to develop and implement effective regulatory strategies for new product registrations, ensuring compliance with local and global regulations.

Responsibilities:

  • Develop and implement regulatory plans for new product registrations, including timelines and submission requirements.
  • Collaborate with cross-functional teams, including product development, manufacturing, and quality assurance, to ensure regulatory compliance.
  • Prepare and submit regulatory documents, including dossiers and labels, to relevant authorities.
  • Maintain accurate records of regulatory submissions, approvals, and post-approval activities.
  • Stay up-to-date with changing regulatory requirements and provide recommendations for process improvements.

Requirements:

  • Bachelor's or Master's degree in a related field, such as pharmacy, chemistry, or biotechnology.
  • Minimum 3 years of experience in regulatory affairs, preferably in the pharmaceutical industry.
  • Strong knowledge of local and global regulatory requirements for pharmaceutical product registration.
  • Excellent communication and project management skills.
  • Ability to work independently and collaboratively as part of a team.

What We Offer:

  • An estimated salary of $85,000 per year, commensurate with experience.
  • A dynamic and supportive work environment.


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