Pfizer Internship for Sciences and Pharmacy Students | Regulatory Affairs

Are you a postgraduate student in Pharmacy or Life Sciences looking for an impactful internship? Pfizer, one of the world’s leading pharmaceutical companies, offers a unique Regulatory Affairs internship opportunity in Chennai. As part of Pfizer’s Global Regulatory Sciences team, you’ll contribute to regulatory strategies that bring breakthrough therapies to patients worldwide.

This internship is a fantastic opportunity to gain hands-on experience and work closely with CMC Global Regulatory Strategists (GRS-CMC) to support regulatory submissions. If you’re eager to be part of a global effort to make life-saving treatments available to those in need, this opportunity is for you!

Why Choose a Pfizer Internship?

At Pfizer, you won’t just be part of a team—you’ll be part of an industry-leading company that is driving forward new therapies that transform patients’ lives. As an intern, you will play a crucial role in ensuring regulatory compliance and support the submission process for the Chemistry, Manufacturing, and Controls (CMC) division. You will help drive new innovations in the pharmaceutical industry while gaining in-depth knowledge of the regulatory landscape.

Location: Chennai, India

Work Type: Hybrid

What You Will Achieve

In this Regulatory Affairs internship, you will assist in the preparation of regulatory submission packages in line with CMC timelines and collaborate with cross-functional teams. Your contribution will help ensure timely submissions to regulatory agencies, keeping Pfizer on track to deliver therapies to patients globally.

This position allows you to:

• Assist in compiling and authoring CMC submission packages under the guidance of Team Leads and Global Regulatory Leaders (GRL).
• Support the review and updating of impacted dossier components.
• Ensure compliance with Pfizer’s internal procedures and regulatory standards.
• Use Pfizer’s advanced systems like GDMS, PDM, and SPA to manage documentation and timelines.

This hands-on role offers you the chance to see firsthand how the pharmaceutical regulatory process works and how critical regulatory affairs are to getting products approved for market.

How You Will Succeed

As an intern, you will:

• Manage your time effectively, ensuring you prioritize tasks to meet deadlines.
• Assist with the day-to-day regulatory activities under the guidance of senior team members.
• Be responsible for escalating any timeline risks or delays to senior leaders.
• Help coordinate internal reviews and documentation sign-off processes.

Your dedication to following established guidelines and your attention to detail will be essential to keeping Pfizer’s regulatory submissions compliant and on schedule.

Qualifications and Skills

Must-Have:

• Postgraduate degree in Pharmacy or Life Sciences.
• Strong attention to detail.
• Good interpersonal communication skills.

Nice-to-Have:

• Basic knowledge of regulatory requirements for post-approval changes in the pharmaceutical industry.
• Experience or understanding of the pharmaceutical manufacturing industry.
• Familiarity with both scientific research environments and the pharmaceutical sector.

This internship provides an excellent opportunity to develop skills in regulatory affairs and gain a comprehensive understanding of Pfizer’s internal processes.

How to Apply

Are you ready to take the next step in your career? Apply now for this Regulatory Affairs internship and start making a difference in the pharmaceutical industry.

To apply, visit the official job posting: Apply Here