Intern Job at Pfizer | Pharmacy Graduates Apply Now
Pfizer is hiring an Intern for its Global Regulatory Sciences – CMC team in Chennai, India. This Intern Job is specifically designed for Postgraduates in Pharmacy or Science who are eager to gain hands-on experience in the pharmaceutical regulatory landscape. The successful candidate will assist the CMC Global Regulatory Strategist in preparing submission packages, managing documentation dossiers, and ensuring strict compliance with global manufacturing and quality standards. This is a prime opportunity to kickstart a career in regulatory affairs with a world leader in biopharmaceuticals.
- Job Posting Title: Intern
- Location: India – Chennai
- Job Requisition ID: 4949392
About The Company
Pfizer is one of the world’s premier biopharmaceutical companies, dedicated to discovering breakthroughs that change patients’ lives. With a global presence, Pfizer applies science and its vast resources to bring transformative therapies to people everywhere, driving the industry forward through innovation, excellence, and a commitment to equity. In Chennai, Pfizer operates key strategic hubs, including the Global Drug Development Center at the IIT Madras Research Park and other specialized facilities that support global regulatory and supply chain operations.
Intern Job Description
A career with us is about discovering breakthroughs that change patients’ lives. You will be part of bringing those therapies to people all over the world, driving the industry forward, and making a positive difference. You will discover that amazing things are possible.
What You Will Achieve
As part of the Global Regulatory Sciences team, you will assist the CMC Global Regulatory Strategist – CMC (GRS-CMC) and collaborate with cross-functional teams to prepare and submit the CMC submission packages as per defined timelines.
Participate in activities related to improving processes of your team and collaborate with others by sharing your experiences. Your knowledge and skills will help in making decisions that make the best of limited options.
It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.
Responsibilities of the Pfizer Job
- Manage own time and professional development, be accountable for own results, and prioritize workflows.
- Assist the CMC strategist in day-to-day regulatory activities associated with assigned activities under the Team Lead’s guidance and supervision.
- Assist in authoring and/or compilation of CMC submission packages under guidance from Team Lead and CMC GRL as appropriate and within agreed timelines.
- Update impacted dossier components as needed.
- Escalate delays in timelines and flag identified risks to the CMC GRL and/or appropriate leadership.
- Coordinate internal document review and sign off.
- Utilize Pfizer’s CMC systems, i.e., GDMS, PDM, SPA, etc., as appropriate.
- Ensure compliance with Pfizer’s internal procedures and training SOPs (PLA).
- Ensure accountability for the highest levels of compliance to norms, policies, and procedures.
Qualifications
- Postgraduate in Pharmacy / Science
- Good attention to detail
- Good interpersonal skills
Aditional Skills
- Knowledge of the Regulatory requirements of post-approval changes
- Basic level of knowledge on general standards, processes, and policies of Pfizer/Pharmaceutical manufacturing Industry
- Understanding of both the pharma industry and the scientific academic research environments
