Pfizer Regulatory Affairs Internship for Pharmacy and MSc Graduates

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

Application Process

Eligible candidates can apply through the official Pfizer careers portal using the link below:

Apply Here: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/Intern_4949392

Applicants are advised to apply early and ensure their profiles highlight academic background, regulatory interest, and attention to detail.

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

Tagged as: Pharma Jobs in Chennai