Pfizer, a global leader in biopharmaceutical innovation, is inviting applications for the position of Intern – Global Regulatory Sciences (CMC) at its Chennai office. This opportunity is ideal for M.Pharm, M.Sc, and other postgraduate science candidates who are looking to gain hands-on exposure in regulatory affairs, CMC documentation, and global submissions within a world-class pharmaceutical organization.

This full-time, hybrid internship allows candidates to work closely with CMC Global Regulatory Strategists, contributing directly to regulatory submissions that support life-changing therapies for patients worldwide.

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Job Overview

• Company: Pfizer
• Position: Intern – Global Regulatory Sciences (CMC)
• Job ID: 4949392
• Location: Chennai, India
• Employment Type: Full Time
• Work Mode: Hybrid / On-Premise
• Industry: Pharmaceutical / Regulatory Affairs
• Experience Required: Fresher / Entry-Level

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Key Responsibilities

As a Regulatory Affairs Intern (CMC) at Pfizer, you will:

• Assist CMC Global Regulatory Strategists in day-to-day regulatory activities
• Support preparation and compilation of CMC submission packages within defined timelines
• Update impacted regulatory dossier components as required
• Coordinate internal document reviews and approval workflows
• Escalate timeline risks and delays to the CMC Global Regulatory Lead
• Utilize Pfizer regulatory systems such as GDMS, PDM, and SPA
• Ensure strict compliance with Pfizer internal SOPs, policies, and training requirements
• Participate in process improvement initiatives within the regulatory team

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Eligibility Criteria

Must-Have Qualifications

• Postgraduate degree in Pharmacy or Science
• High attention to detail
• Strong interpersonal and communication skills

Nice-to-Have Skills

• Basic knowledge of post-approval regulatory requirements
• Understanding of pharmaceutical manufacturing and regulatory processes
• Familiarity with scientific research and pharma industry standards

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Why Join Pfizer?

• Work with a globally respected pharmaceutical company
• Gain real-world exposure to Global Regulatory Affairs (CMC)
• Learn directly from experienced regulatory professionals
• Contribute to therapies that improve and save patient lives worldwide
• Enhance career prospects in Regulatory Affairs, CMC, and Clinical Documentation

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Stipend / Salary (Estimated)

• ₹15,000 – ₹25,000 per month (Indicative, based on industry standards for pharma internships)

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How to Apply

Application Link