Explore high-paying Regulatory Writing jobs at Eli Lilly Bengaluru. Open roles for Associate, Senior Associate, and Lead positions in R&D. Apply now to join a global pharma leader!
🧬 Eli Lilly and Company is Hiring – Associate/Senior Associate/Lead in Regulatory Writing | Bengaluru R&D Center
Are you an experienced regulatory writer or medical writing professional looking for high-paying jobs in India’s pharma sector? Eli Lilly and Company – a global healthcare leader – is hiring for multiple roles in Regulatory Writing at its Research & Development center in Bengaluru. These full-time roles are ideal for candidates in life sciences, medical writing, or clinical research seeking top-notch growth and global exposure.
🌍 About Eli Lilly and Company
Founded in 1876 and headquartered in Indianapolis, Indiana, Eli Lilly and Company is a Fortune 500 biopharmaceutical giant with a presence in over 18 countries. With more than 35,000 employees worldwide, the company specializes in oncology, diabetes, immunology, and neuroscience. Eli Lilly’s Bengaluru R&D center plays a vital role in global clinical development, regulatory writing, and regulatory affairs.
- Glassdoor Rating: ★★★★☆
- AmbitionBox Job Security Rating: 3.9/5
- Average Salary: ₹15–18 LPA for Regulatory Writing professionals.
🧾 Current Openings: Regulatory Writing – Associate/Senior Associate/Lead
- Job ID: R-87544
- Location: Bengaluru, Karnataka, India
- Department: Research & Development (R&D)
- Job Type: Full-time, Regular
- Application Deadline: Rolling until filled
- Application Portal: careers.lilly.com
📌 Position Overview
The role of Scientific Communications Associate – Regulatory Writing involves creating, managing, and delivering high-quality clinical and regulatory documents that support product development, clinical trials, and global health authority submissions.
These roles demand a solid understanding of regulatory frameworks (ICH, FDA, EMA), excellent writing skills, and the ability to collaborate with cross-functional global teams.
🎯 Key Responsibilities
🔍 Content Creation & Regulatory Strategy
- Write and edit clinical trial protocols, amendments, informed consent forms (ICFs), Investigator Brochures, and regulatory response documents.
- Develop content strategies ensuring accuracy, clarity, and compliance with international regulatory standards.
- Ensure alignment and consistency across related documents and product dossiers.
👥 Project Management & Collaboration
- Act as the primary author and content lead for assigned documents.
- Coordinate with clinical teams, statisticians, regulatory affairs, and external vendors.
- Manage timelines, reviews, quality checks, and version control.
📚 Skill Development & Industry Awareness
- Stay current with evolving therapeutic area knowledge, regulatory guidelines (e.g., FDA, EMA, PMDA), and industry best practices.
- Participate in training sessions and mentoring programs for junior writers.
✅ Eligibility Criteria
📘 Education:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, Biotechnology, Communications, or related fields.
💼 Experience:
- Required: Minimum 2–5 years of professional regulatory writing experience.
- Preferred:
- Graduate degree with research experience
- Experience in oncology, neuroscience, or immunology
- Exposure to clinical pharmacology and medical affairs documentation
✍️ Skills:
- Proficient in scientific and regulatory writing with excellent grammar and attention to detail.
- Strong interpersonal skills and stakeholder management.
- Familiarity with MS Word templates, referencing tools (e.g., EndNote), and document management systems.
- Mandatory writing test during recruitment.
💼 Why Work at Eli Lilly?
💰 Competitive Compensation & Benefits:
- Average salary: ₹15,58,999 annually
- Performance bonuses, stock options, and healthcare benefits
- Access to learning & development platforms, leadership training
🌱 Career Growth:
- Work on global regulatory submissions, interact with global teams, and learn from seasoned regulatory experts
- Career paths leading to Medical Affairs, Clinical Development, or Regulatory Strategy
🧠 Work Culture:
- Collaborative, innovation-focused, and employee-friendly
- Great Place to Work® Certified
- Committed to diversity, equity, and inclusion
📍 Why Bengaluru – The R&D Capital of India?
Bengaluru’s thriving pharma and biotech ecosystem makes it the ideal destination for professionals seeking meaningful, high-paying jobs in India’s pharmaceutical sector. Eli Lilly’s office is located in Electronic City, easily accessible via major routes.
📝 How to Apply
✔️ Step-by-Step Application:
- Visit careers.lilly.com
- Search Job ID R-87544 or “Regulatory Writing Bengaluru”
- Upload:
- Updated resume
- Copies of education & experience certificates
- PAN & Aadhaar Card (for Indian candidates)
- Complete the mandatory writing exercise
💡 Need Accommodation?
Fill out the workplace accommodation form for disability-related support.
⚠️ Important Notes
- No application fees required – Beware of job scams. Report suspicious activity to cybercrime.gov.in.
- Candidates interviewed in the last 6 months are not eligible to reapply.
- This role may involve tight deadlines and high-pressure environments with immense learning potential.
🚀 Apply Today!
Don’t miss this exclusive opportunity to work with a global pharmaceutical leader and contribute to life-changing therapies. Apply now at careers.lilly.com and join Eli Lilly in making science accessible, meaningful, and impactful.
