Lilly Regulatory Intern

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life‑changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first.

We’re looking for people who are determined to make life better for people around the world.

Lilly StarT is a one‑year talent program designed for junior and senior university students in relevant fields of study, offering an opportunity to join our business functions.

The program aims to grow exceptional talents who are eager to take ownership of their professional journey and emerge as future leaders in the pharma sector.

With Lilly StarT, you will collaborate closely with cross‑functional teams, engage with experts in the field, build strong relationships, and take an active role in project assignments — all while receiving on‑the‑job training, online and in‑class development opportunities, and gaining hands‑on experience.

• Creating and maintaining the department’s archive system
• Responding to queries on regulatory processes and product regulatory status
• Supporting the preparation and submission of applications to the local regulatory agency — including new products, line extensions, variations (CMC, new indications, labelling), renewals, co‑marketing applications, and GMP submissions for inspections — to help obtain and maintain product licenses
• Monitoring regulatory updates issued by local and international authorities, communicating relevant changes to internal stakeholders, and supporting the implementation of required actions

• 4th or 5th year Pharmacy student from a reputable university
• Good command of English (written and verbal)
• Strong planning, priority‑setting, and organizational skills
• Critical thinking and problem‑solving ability
• Proactive attitude with high learning agility and openness to coaching and feedback
• Strong teamwork and interpersonal skills
• Resilience and adaptability in the face of change
• Proficiency in MS Office programs and AI tools
• Attention to detail and ability to track multiple tasks and deadlines simultaneously
• Interest in pharmaceutical regulatory affairs and willingness to learn regulatory processes
• Available to work full‑time during the summer break and at least 3 days per week during the school term

Lilly is a medicine company turning science into healing to make life better for people around the world. Lilly started its operations in Türkiye in the 1950s by having its products manufactured and distributed through a partnership with a Turkish company. In 1993, its operations were gathered under Lilly İlaç Ticaret Ltd. Şti. Since then, Lilly has been bringing discoveries in the therapeutic areas of endocrinology, central nervous system diseases, oncology, dermatology, rheumatology, migraine, and men’s health to the people of Türkiye.

Lilly İlaç has been recognized as a Top Employer in Türkiye multiple times and was included among Türkiye’s Best Employers in Aon Hewitt’s Best Employer Surveys on three occasions. Following Great Place to Work® certification in 2023 and 2024, Lilly İlaç was named to the Türkiye’s Best Employers™ 2025 list by Great Place to Work®. Additionally, Lilly İlaç has been honored with the ETIKA Türkiye Ethics Awards by EDMER eleven consecutive times.

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