Pharmacovigilance Regulatory Intelligence Internship

About the internship

This work-from-home internship is focused on monitoring global pharmacovigilance and regulatory intelligence sources and checking whether the platform accurately captures and summarizes important updates. The role is designed for someone who can handle detail-heavy review work, assess regulatory relevance, and help keep the content accurate, current, and useful for specialist users.

What you will do

• Track official updates from key pharmacovigilance, regulatory, health authority, and medical device safety sources, including the FDA, EMA, MHRA, Health Canada, TGA, HSA, Swissmedic, SFDA, and other international regulators.
• Check whether new updates are being captured correctly, including the title, source, country or region, date, update category, urgency, affected PV functions, workflow relevance, and the action required.
• Review AI-created or system-created summaries and verify that they match the original regulatory source before anything is published or escalated.
• Sort updates by their pharmacovigilance significance, such as ICSR reporting, signal detection, risk management, labeling, local affiliate compliance, device vigilance, inspection readiness, AI/GxP governance, and broader regulatory intelligence monitoring.
• Write short impact notes that explain why an update matters, who it affects, and what action a PV, regulatory, or compliance team may need to consider.
• Keep a daily record of the sources reviewed, updates identified, updates captured by the system, missed items, incorrect classifications, duplicates, and items that still need review.
• Support preparation of weekly digests by highlighting the most important updates for users such as the QPPV, Regulatory Intelligence Lead, Signal Management Lead, PV Quality Lead, and Device Vigilance Lead.
• Share structured feedback to improve content quality, tagging accuracy, site freshness, and overall relevance by flagging gaps, outdated entries, unclear summaries, and missed regulatory updates.

Who can apply

This opportunity is open to candidates who are available for a remote internship, can begin between 30 June 2026 and 4 August 2026, can commit to the full 6-month duration, and have relevant skills and interest in the area.

Other requirements

• A background in B.Pharm, M.Pharm, Pharm.D, MSc Life Sciences, Biotechnology, Clinical Research, Regulatory Affairs, or a related discipline is preferred.
• Basic familiarity with pharmacovigilance, regulatory affairs, drug safety, clinical safety, or medical device vigilance is preferred.
• You should be comfortable reviewing official regulator websites, guidance material, safety alerts, recalls, public notices, and regulatory announcements.
• Strong attention to detail is important, along with the ability to tell apart general healthcare news from PV-relevant regulatory intelligence.

Perks

• Certificate
• Letter of recommendation
• Flexible work hours
• 5-day work week

About the company

The company is a digital solutions partner that builds custom software and mobile/web applications and provides IT consulting for digital transformation. It works across healthcare and e-commerce with an agile approach, domain expertise, customer-focused delivery, clear SLAs, and dedicated success managers. It also works with emerging technologies such as AI/ML, IoT, and blockchain.

Additional information

Stipend: INR 10,000 to 15,000 per month.

Location: Work from home. The listed city is Noida, Uttar Pradesh, India.

Application deadline: 30 July 2026, 11:59:59 PM.

Vacancies: 1.