Medical Writing Jobs 2026 | Lilly Hiring Scientific Writer – Toxicology & Non-Clinical Submissions

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Scientific Writer – Toxicology & Non-Clinical Submissions

🏢 Eli Lilly & Company

📍 Bengaluru

🎓 M.Pharm | Pharm.D | Life Sciences

💼 2–4 Years

Eli Lilly and Company is hiring a Scientific Writer – Global Scientific Communications Toxicology & Non-Clinical Submissions in Bengaluru. This opportunity is ideal for professionals with experience in Scientific Writing, Regulatory Writing, Toxicology Documentation, IND Submissions, eCTD Publishing, ADME Reporting, and Non-Clinical Drug Development.

📋 Job Overview

Particulars	Details
Position	Scientific Writer – Toxicology & Non-Clinical Submissions
Company	Eli Lilly and Company
Location	Bengaluru
Department	Global Scientific Communications
Job ID	R-106747
Application Deadline	30 June 2026

✍️ Scientific Writing Responsibilities

Plan, write, review, and finalize non-clinical scientific documents.
Prepare toxicology and ADME study reports.
Develop scientific content using approved templates.
Ensure scientific accuracy and regulatory compliance.
Maintain consistency across regulatory documents.
Support document review and approval workflows.

📑 Regulatory Submission Responsibilities

Support IND submission activities.
Assist with Marketing Authorization Applications (MAA).
Prepare briefing books and regulatory responses.
Coordinate non-clinical submission deliverables.
Manage eCTD document content and publishing activities.
Support global regulatory documentation requirements.

📊 Project Management Responsibilities

Manage document timelines and milestones.
Coordinate cross-functional scientific reviews.
Track submission deliverables and deadlines.
Identify project risks and mitigation plans.
Communicate project progress with stakeholders.

🤝 Cross-Functional Collaboration

Toxicology Scientists
ADME Scientists
Pathologists
PK Scientists
PD Scientists
Discovery Biologists
Environmental Risk Assessment Teams
Regulatory Affairs Professionals

🎓 Eligible Qualifications

M.Pharm
Pharm.D
M.Sc Life Sciences
Biotechnology
Toxicology
Pharmacology
Biomedical Sciences
Related Scientific Disciplines

💡 Preferred Skills

Scientific Writing
Regulatory Writing
Toxicology Documentation
Non-Clinical Study Reports
IND Submissions
eCTD Publishing
ADME Documentation
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Project Management

🌟 Why Join Lilly?

Work on global drug development programs.
Exposure to worldwide regulatory submissions.
Collaborative scientific environment.
Career growth in Medical & Regulatory Writing.
Learning and development opportunities.
Work with one of the world's leading pharmaceutical companies.

📈 Career Path

Scientific Writer
Senior Scientific Writer
Regulatory Writing Specialist
Principal Scientific Writer
Medical Writing Manager
Associate Director – Scientific Communications
Director – Regulatory & Scientific Writing

📝 Resume Tips

Highlight scientific and regulatory writing experience.
Mention IND, MAA, NDA, or eCTD submission exposure.
Include toxicology, ADME, PK, and PD documentation experience.
Showcase project management and stakeholder coordination skills.
Mention publication, report writing, or regulatory submission projects.
Keep your resume ATS-friendly and achievement-focused.

🎯 Interview Preparation Tips

Revise non-clinical drug development processes.
Understand toxicology and ADME study documentation.
Review IND and MAA submission requirements.
Learn eCTD structure and publishing concepts.
Prepare examples demonstrating scientific writing expertise.
Review project management and timeline management scenarios.
Research Lilly's therapeutic areas and pipeline.

❓ Common Interview Questions

What is the purpose of an IND submission?
Explain the structure of an eCTD submission.
What is ADME and why is it important?
How do you ensure scientific accuracy in reports?
What are the key sections of a toxicology study report?
How do you manage multiple document deadlines?
Describe your experience with regulatory writing.
How do you handle reviewer comments and document revisions?
What challenges have you faced in scientific writing projects?
Why do you want to join Lilly?

❓ Frequently Asked Questions (FAQ)

Q1. Which location is hiring?
Bengaluru, Karnataka.

Q2. What experience is required?
Typically 2–4 years of scientific or regulatory writing experience.

Q3. Which qualifications are eligible?
M.Pharm, Pharm.D, M.Sc Life Sciences, Biotechnology, Toxicology, Pharmacology, Biomedical Sciences, and related disciplines.

Q4. Is regulatory writing experience preferred?
Yes, experience in scientific writing, regulatory documentation, and submissions is highly valuable.

Q5. What is the application deadline?
30 June 2026.

📝 How to Apply

Review the complete job description carefully.
Update your resume with scientific writing and regulatory submission experience.
Highlight toxicology, ADME, PK/PD, and eCTD exposure.
Showcase project management and cross-functional collaboration experience.
Apply only if your qualifications align with the role requirements.

👉 Step-by-Step Guide: How to Apply for Healthcare & Pharma Jobs