manager drug regulatory affairs

1 week ago

Ludhiana, Punjab, India Randstad MENA Full time ₹ 1,20,000 - ₹ 1,80,000 per year
Job Description

Job Offer Closes: 8 December 2025

Summary

  • Location: Ludhiana, Punjab
  • Company: A client of Randstad India
  • Employment Type: Permanent
  • Posted On: 9 October 2025

Reference Number: JPC

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Job Details

Position: Drug Regulatory Affairs (Domestic Market)
Location: Ludhiana, Punjab, India
Salary: Competitive Salary
Employment Type: Full Time
Required Qualification: M-Pharma

We are seeking an experienced and dedicated Drug Regulatory Affairs professional to join our dynamic team. This is a full-time position focused on managing domestic market regulatory submissions and ensuring compliance with all relevant Indian regulations. As a Drug Regulatory Affairs specialist, you will play a critical role in bringing life-saving and life-enhancing products to market efficiently and safely. If you have a strong background in drug regulatory affairs and a proactive approach, we encourage you to apply for this exciting opportunity as a Drug Regulatory Affairs professional.

What do we offer you?
  • Competitive pay
  • Growth path
  • Skill enhancement
  • Engaging work
  • Team spirit
  • Meaningful tasks
Who are you?

We are looking for a highly motivated individual with a strong understanding of the Indian regulatory landscape. The ideal candidate will possess:

  • M-Pharma degree or equivalent
  • 10-18 years of experience in Drug Regulatory Affairs
  • Expertise in CDSCO regulations
  • Excellent communication skills
  • Proactive and detail-oriented approach
What are you going to do?

In this role as a Drug Regulatory Affairs professional, your responsibilities will include:

  • Preparing and submitting regulatory dossiers to CDSCO and other relevant authorities.
  • Ensuring compliance with domestic market regulations for all product lifecycle stages.
  • Interacting with regulatory agencies and responding to queries.
  • Monitoring regulatory changes and implementing necessary updates.
  • Providing regulatory guidance to cross-functional teams.
  • Contributing to the strategic planning of regulatory affairs.
Where are you going to work?

You will be working with a leading pharmaceutical company dedicated to innovation and patient well-being. Our client is committed to fostering a supportive and collaborative work environment. As a Drug Regulatory Affairs specialist, you will be an integral part of our client's success.

If you are a seasoned Drug Regulatory Affairs professional looking for a challenging and rewarding role, we want to hear from you. Apply now to become our next Drug Regulatory Affairs expert

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