Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization
Eli Lilly · Bengaluru
- Experience3–4 yrs
- SalaryNot disclosed
- Work modeonsite
- Posted25 Sept 2026
About Eli Lilly
Eli Lilly is hiring in Bengaluru in pharma biotech. This role looks for around 3+ years of experience.
Skills
- eCTD
- Microsoft Word
- Microsoft Excel
- medical terminology
- statistical terminology
- English
The role
A technical writer at a pharmaceutical company produces medical regulatory documents using eCTD-compliant PDFs, scientific literature, and medical terminology. The role reviews scientific content, applies document standards, and finalizes publication-ready materials.
Full job description
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Purpose:
The purpose of the Scientific Writer/Senior Scientific Writer role (Quality review and document finalization) is to support the Global Scientific Communications team and other functions to produce documents of high quality.
Primary Responsibilities:
Scientific Communications Document Support
Ensure timely delivery of error-free, high-quality documents that meet international standards of written English
Correct errors in grammar, style, formatting, and syntax. Identify and fix flaws in logic and flow
Follow style guides/templates provided by the team
Follow best-practice based on Lilly internal standards
Verify data against source files, ensure accuracy and consistency of data and content within and between related documents
Document finalization/publishing services
Produce final eCTD-compliant PDFs of medical regulatory documents using publishing software
Review and format Word files to ensure as many compliance requirements are in the source file as possible
Render the Word files into PDFs
Review the PDFs and edit them as needed to ensure that all regulatory requirements are met
General expectations
Maintain a strong customer focus
Accountable for achieving timelines by managing activities efficiently and proactively; utilize ability to understand and apply team communication strategies to work products
Coach new staff or others requiring development in core areas
Coordinate with vendors if any of the aforementioned activities are outsourced
Process efficiency and technology advancement
Maintain proficiency in applicable software, tools, processes, and workflows
Use creativity to introduce new tools, processes, and structure to accomplish broader organizational goals and meet standards while providing solutions to streamline team workflow
Improve document processes by establishing uniform cross-organizational practices; suggest process or tool enhancements to improve effectiveness and minimize redundancy between databases and other tools
undefined
Therapeutic & Disease State Management
Understand key priorities and communication strategies across therapeutic areas and/or organizational units
Maintain a working knowledge of product and disease state information
Continue to develop therapeutic knowledge and be familiar with trial design, rationale and data. Apply this knowledge in activities listed above
Minimum Qualification Requirements:
Bachelor's degree
Strong written and verbal communication skills in English
Demonstrated ability to communicate and negotiate solutions to complex technical challenges with cross-functional colleagues, external vendors and customers
Demonstrated project management and time management skills
Cognitive abilities, including verbal reasoning, attention to detail, critical thinking, and analytical ability
Interpersonal skills and the ability to be flexible in varying environments
Ability to utilize high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentations and templates)
Ability to work well independently and as part of a team, within and across culturally and geographically diverse environments
Proven ability to assemble, share and apply key learnings across multiple projects
Other Information/Additional Preferences:
Knowledge of medical and statistical terminology; willingness to expend effort in acquiring scientific knowledge and understand strategic issues
General knowledge of scientific literature search and retrieval
Limited travel, up to approximately 10%
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#WeAreLilly