Regulatory Affairs Jobs at Lupin | MSc Chemistry Candidates Apply Now

Regulatory Affairs Jobs at Lupin | MSc Chemistry Freshers Apply Now

Regulatory Affairs Jobs at Lupin. Starting a career in Regulatory Affairs becomes far more rewarding when you begin with a globally trusted pharmaceutical leader like Lupin. This role offers hands-on experience in regulatory submissions, labeling updates, dossier compilation, and product launch support—making it an ideal opportunity for freshers and early-career professionals looking to grow in a high-impact regulatory environment. Interested candidates apply for the exciting opportunity at Lupin Careers. Freshers Jobs at Lupin.

About Lupin:

Lupin is a global pharmaceutical company renowned for its dedication to improving health and well-being. We are driven by the mission to deliver affordable and accessible medication to millions worldwide. Our innovative approach and commitment to research and development make us a leader in the industry.

  • Job Title: Officer – RA
  • Date: Nov 20, 2025
  • Location: Santacruz, MH, IN
  • Company: Lupin

Job Description:

  • Replacement for Manisha Shivpuje
  • To support the activities for Regulatory Submissions as given below:
    • Submission of Annual Reports and supplements.
    • Support for New Product Launch.
    • Submission of Labeling Amendment.
    • Submission of Response to DRL (Discipline Review Letter)/IR (Information Request), Complete Response Amendment Support

Work Experience:

  • Fresher to 1 year. Dossier compilation experience / Awareness on quality guidelines.

Education:

  • Graduation in Pharmacy
  • Master’s in Chemistry

Competencies:

  • Customer Centricity
  • Developing Talent
  • Collaboration
  • Strategic Agility
  • Process Excellence
  • Stakeholder Management
  • Innovation & Creativity
  • Result Orientation

Why Should You Join?

Joining as an Officer in Regulatory Affairs at Lupin gives you the chance to build a strong foundation in global regulatory processes while working with experienced industry professionals. You gain hands-on exposure to submissions, labeling updates, and dossier compilation—skills that fast-track your growth in one of the most in-demand pharmaceutical domains. This role empowers you to learn, contribute, and build a future-ready regulatory career from day one.

APPLY ONLINE HERE

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