Pfizer Regulatory Affairs Internship for Pharmacy and MSc Graduates

Pfizer Healthcare India; Chennai District; On-site; INR 167,000 - 279,000; Full time

Job summary

Pfizer is hiring Pharmacy and science postgraduates for Regulatory Affairs Intern roles in Chennai. The internship provides hands‑on exposure to regulatory affairs, CMC submissions, and global pharmaceutical compliance within the Global Regulatory Sciences - CMC team.

Roles are in a hybrid, full-time internship setting. Responsibilities include assisting with CMC submission packages, coordinating document reviews, and ensuring data integrity across regulatory documentation.

Qualifications

• Must have postgraduate qualification in Pharmacy or Science.
• Strong attention to detail and documentation accuracy.
• Excellent interpersonal and written communication skills.
• Ability to work in structured, compliance-driven environments.

Responsibilities

• Support CMC Global Regulatory Strategists in day-to-day regulatory activities under team lead supervision.
• Assist in authoring and compiling CMC submission packages within agreed timelines.
• Update dossier components based on regulatory or manufacturing changes.
• Coordinate internal document reviews and approval sign-offs.
• Escalate timeline risks or delays to the CMC GRL and leadership.
• Use Pfizer regulatory systems such as GDMS, PDM, and SPA.

Skills

Attention to detail

Interpersonal skills

Structured/compliance mindset

Education

Postgraduate qualification in Pharmacy or Science

Job description

Pharmacy Postgraduates Hiring - Regulatory Affairs Intern, Chennai

Pharmacy and science postgraduates hiring for Regulatory Affairs Intern at Pfizer. Multiple intern positions, Chennai hybrid role.

Pfizer is offering a full-time Intern opportunity within its Global Regulatory Sciences - CMC team in Chennai. This role is designed for postgraduate pharmacy and science candidates who want real-world exposure to regulatory affairs, CMC submissions, and global pharmaceutical compliance. The internship provides hands‑on experience in regulatory documentation, dossier preparation, and cross‑functional collaboration within a global biopharmaceutical organization.

Company Overview

Pfizer is one of the world’s most respected biopharmaceutical companies, driven by a clear mission to deliver breakthroughs that change patients’ lives. With a strong presence across drug development, regulatory sciences, manufacturing, and global submissions, Pfizer sets industry benchmarks for quality, compliance, and scientific excellence.

Every role at Pfizer contributes to advancing therapies that reach patients worldwide. The organization operates with strict regulatory standards, robust internal systems, and a strong culture of ethics and accountability, making it a highly trusted employer for professionals building careers in pharmaceutical and regulatory sciences.

Job Role & Responsibilities

As a Regulatory Affairs Intern within the Global Regulatory Sciences - CMC function, you will support regulatory strategists in preparing and managing Chemistry, Manufacturing, and Controls (CMC) submission activities. This role emphasizes learning, compliance, and contribution to live regulatory projects.

Core Responsibilities

• Support CMC Global Regulatory Strategists in day-to-day regulatory activities under team lead supervision
• Assist in authoring and compiling CMC submission packages within agreed timelines
• Update impacted dossier components based on regulatory or manufacturing changes
• Coordinate internal document reviews and approval sign-offs
• Escalate timeline risks or delays to the CMC GRL and appropriate leadership
• Use Pfizer regulatory and document management systems such as GDMS, PDM, and SPA
• Ensure compliance with Pfizer internal procedures, training requirements, and SOPs (PLA)
• Maintain high standards of regulatory compliance, documentation accuracy, and data integrity

Process Improvement & Collaboration

• Participate in initiatives to improve regulatory and submission processes
• Collaborate with cross-functional teams by sharing observations and learnings
• Manage personal workload, timelines, and professional development effectively

This internship plays a supporting role in ensuring timely and compliant global regulatory submissions that directly impact product lifecycle management and patient access.

Eligibility / Qualifications

Educational Background

Candidates must meet the following criteria:

• Postgraduate qualification in Pharmacy or Science

Relevant courses include:
MPharmacy, MSc Pharmaceutical Sciences, MSc Chemistry, MSc Biotechnology, MSc Life Sciences, MSc Regulatory Affairs, MSc Industrial Pharmacy

Must-Have Skills

• High attention to detail and documentation accuracy
• Strong interpersonal and communication skills
• Ability to work in structured, compliance-driven environments

Nice-to-Have Skills

• Basic knowledge of regulatory requirements related to post-approval changes
• Understanding of pharmaceutical manufacturing and regulatory processes
• Familiarity with pharma industry practices and academic research environments

Location & Salary

• Job Location: Chennai, Tamil Nadu
• Work Mode: Hybrid / On-Premise
• Employment Type: Full-time Intern
• Weekly Hours: 40

Frequently Asked Questions (FAQs)

Who can apply for this Pfizer internship?

Postgraduate pharmacy and science candidates with interest in regulatory affairs and pharmaceutical compliance can apply.

Is this internship suitable for MPharmacy students?

Yes. MPharmacy and MSc graduates with regulatory or pharmaceutical science backgrounds are ideal candidates.

Is this a paid internship?

Pfizer has not disclosed stipend details. Compensation will follow company internship policies.

Is the internship remote or on-site?

This role follows a hybrid or on-premise work model based in Chennai.

Does this internship involve regulatory submissions?

Yes. Interns will assist with CMC submission packages and regulatory documentation.

Vertical Summary Table

• Company: Pfizer
• Vacancies: Regulatory Affairs Intern - Global Regulatory Sciences CMC (Multiple Positions)
• Required Education: MPharmacy, MSc Pharmaceutical Sciences, MSc Chemistry, MSc Biotechnology, MSc Life Sciences, MSc Regulatory Affairs
• Experience: Fresher / Academic exposure to regulatory or pharmaceutical sciences