Pfizer is one of the world’s largest and most innovative pharmaceutical companies, committed to discovering and developing breakthroughs that change patients’ lives. With a long-standing history of making a global impact in healthcare, Pfizer’s mission is to bring therapies to people in need around the world. As a part of the Pfizer team, you will play a crucial role in advancing the pharmaceutical industry and improving patient outcomes.
Responsibilities in the Job: As an intern in the Global Regulatory Sciences team at Pfizer, you will have the opportunity to assist the CMC (Chemistry, Manufacturing, and Controls) Global Regulatory Strategist and work closely with cross-functional teams. Your responsibilities will include:
- Assisting in day-to-day regulatory activities under the guidance of the Team Lead.
- Compiling and submitting CMC submission packages in line with established timelines.
- Updating dossier components and escalating any delays or risks to leadership.
- Coordinating internal document reviews and ensuring sign-off.
- Using Pfizer’s CMC systems, such as GDMS, PDM, and SPA, to maintain data and documentation.
- Ensuring compliance with Pfizer’s internal procedures, policies, and training SOPs.
Qualifications: To be eligible for this internship, you should have:
- A postgraduate degree in Pharmacy or Science.
- High attention to detail and the ability to work efficiently within a structured environment.
- A good understanding of both the pharmaceutical industry and scientific research environments.
Skills:
- Strong interpersonal and communication skills.
- Knowledge of regulatory requirements for post-approval changes is advantageous.
- Familiarity with general pharmaceutical industry standards, processes, and policies.
