Pfizer has announced an Intern job opportunity in Chennai for candidates interested in regulatory support, pharmaceutical documentation, CMC activities and tender support operations. This full-time, on-premise opportunity provides exposure to global pharmaceutical regulatory processes and Pfizer’s internal CMC and document-management systems.
The Pfizer Intern Chennai job involves reviewing regulatory documents, supporting tender requests, checking product registration information and coordinating CMC documentation. Candidates with knowledge of CTD documents, CMC documentation and Module 3 may find this opportunity particularly relevant.
The official job description does not specify a mandatory educational qualification or experience requirement. Candidates should therefore verify their eligibility on the official Pfizer Careers application page before applying.
Key Responsibilities
Selected candidates for the Pfizer Intern position will support regulatory and tender-related activities, including:
- Review documents received from requestors through email, GDMS, GTCS and relevant tender-support channels.
- Manage day-to-day regulatory activities within agreed timelines.
- Evaluate tender requests for completeness, accuracy and availability of required supporting documents.
- Communicate with requestors when additional or corrected tender documentation is required.
- Review PEARL to determine whether a product is registered in the relevant market.
- Cross-check product registration information against PDM.
- Retrieve required ancillary documents through the SPA system.
- Coordinate with relevant stakeholders and provide requested documents within established timelines.
- Continuously monitor SPA to prevent ancillary requests from crossing due dates.
- Handle urgent ancillary requests where rapid business support is required.
- Work with CTD and CMC documentation, particularly Module 3 documents and CMC ancillaries.
- Use Pfizer CMC systems such as GDMS, PDM and ARS SharePoint where appropriate.
- Follow Pfizer internal procedures, SOPs and applicable training requirements.
- Perform other responsibilities assigned by line managers.
Skills and Knowledge Required
The role requires strong pharmaceutical documentation and regulatory-support capabilities. Important competencies highlighted in the job description include:
CTD Documentation: Knowledge of Common Technical Document requirements is described as essential.
CMC & Module 3: Understanding of Chemistry, Manufacturing and Controls documentation, including Module 3 and CMC ancillaries, is important.
Regulatory Operations: Candidates should be capable of managing regulatory support activities within established timelines.
Attention to Detail: High accuracy is necessary when reviewing registration information, tender requests and supporting documentation.
Time Management: Tender requests can arrive at short notice, making prioritization and organization important.
Change Agility: Candidates should be comfortable adapting to changing business priorities and urgent requests.
Qualification & Eligibility
Pfizer’s supplied job description does not specify a mandatory degree or academic qualification for this Intern position.
However, based on the regulatory/CMC nature of the work, candidates from pharmaceutical or relevant life-science educational backgrounds may find their academic knowledge useful. Applicants should not assume eligibility solely based on degree and should check the official Pfizer Careers listing for any additional screening requirements.
Knowledge of the following areas is particularly relevant:
- CTD documentation
- CMC documentation
- Module 3
- Regulatory documentation
- Pharmaceutical product registration
- Tender support
- Document management
- SOP compliance
- Regulatory systems and databases
Why Consider This Pfizer Internship?
The Pfizer Intern job in Chennai provides an opportunity to gain practical exposure to regulatory documentation and pharmaceutical business-support activities within a global biopharmaceutical organization.
Potential professional exposure includes CMC documentation, product registration verification, tender support, global regulatory systems, stakeholder coordination, SOP-driven processes and time-sensitive pharmaceutical documentation.
This experience can be particularly useful for candidates seeking to develop careers in areas such as Regulatory Affairs, Regulatory Operations, CMC Regulatory Affairs, pharmaceutical documentation and regulatory support services.
Salary
Pfizer has not disclosed compensation for this Intern position in the provided job posting.
For structured-data purposes, an estimated salary range of approximately ₹3,00,000–₹5,00,000 per year may be used only when clearly identified as an estimate and if permitted by the source/job-board policy. Applicants should rely on Pfizer for the actual compensation offered during recruitment.
Work Location
Chennai, Tamil Nadu, India
The position is designated as On Premise, meaning selected candidates should expect to work from the assigned Pfizer workplace rather than as a fully remote employee.
How to Apply
