Lilly

healthcare

RegulatoryInternAnkara

Istanbul, Turkey; Turkey PART TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Regulatory Intern – Ankara at Lilly. Skills: pharmaceutical regulatory affairs. Creating and maintaining the department 's archive system. Responding to queries on regulatory processes and product regulatory status”

What You'll Achieve.

obtain and maintain product licenses

Industry & Context.

healthcare
Problems you'll solve

Critical thinking and problem-solving ability

Eligibility Requirements

Available to work full-time during the summer break and at least 3 days per week during the school term

What They're Looking For.

Must Have

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

What You'll Do.

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

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

How You'll Work.

Team & Collaboration

collaborate closely with cross-functional teams; engage with experts in the field; build relationships

Communication Scope

Good command of English (written and verbal)

Process & Methodology

track multiple tasks and deadlines simultaneously

Full Job Description

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. **What is Lilly StarT?** **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.** **Role: Regulatory Intern – Ankara** **As a Regulatory Intern, you will support the Regulatory team by:** * **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** **Requirements** * *

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