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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.
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
Key Responsibilities
As a Regulatory Affairs Intern (CMC) at Pfizer, you will:
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- 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
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
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
Stipend / Salary (Estimated)
- ₹15,000 – ₹25,000 per month (Indicative, based on industry standards for pharma internships)
How to Apply
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