Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization

Eli Lilly and Company · Bengaluru East

  • Experience3–4 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Posted25 Sept 2026

About Eli Lilly and Company

Eli Lilly and Company is hiring in Bengaluru East in pharma biotech. This role looks for around 3+ years of experience.

Skills

  • medical writing
  • regulatory publishing
  • eCTD
  • publishing software
  • Microsoft Word
  • English

The role

A scientific writer at a pharmaceutical company edits medical regulatory documents, applies medical writing and regulatory publishing, and finalizes eCTD-compliant PDFs using publishing software. The role also verifies clinical data and maintains scientific literature search skills.

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 SupportEnsure timely delivery of error-free, high-quality documents that meet international standards of written EnglishCorrect errors in grammar, style, formatting, and syntax. Identify and fix flaws in logic and flowFollow style guides/templates provided by the teamFollow best-practice based on Lilly internal standardsVerify data against source files, ensure accuracy and consistency of data and content within and between related documentsDocument finalization/publishing servicesProduce final eCTD-compliant PDFs of medical regulatory documents using publishing softwareReview and format Word files to ensure as many compliance requirements are in the source file as possibleRender the Word files into PDFsReview the PDFs and edit them as needed to ensure that all regulatory requirements are met

General expectations

Maintain a strong customer focusAccountable for achieving timelines by managing activities efficiently and proactively; utilize ability to understand and apply team communication strategies to work productsCoach new staff or others requiring development in core areasCoordinate with vendors if any of the aforementioned activities are outsourced

Process efficiency and technology advancement

Maintain proficiency in applicable software, tools, processes, and workflowsUse creativity to introduce new tools, processes, and structure to accomplish broader organizational goals and meet standards while providing solutions to streamline team workflowImprove document processes by establishing uniform cross-organizational practices; suggest process or tool enhancements to improve effectiveness and minimize redundancy between databases and other toolsundefined

Therapeutic & Disease State Management

Understand key priorities and communication strategies across therapeutic areas and/or organizational unitsMaintain a working knowledge of product and disease state informationContinue 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 degreeStrong written and verbal communication skills in EnglishDemonstrated ability to communicate and negotiate solutions to complex technical challenges with cross-functional colleagues, external vendors and customersDemonstrated project management and time management skillsCognitive abilities, including verbal reasoning, attention to detail, critical thinking, and analytical abilityInterpersonal skills and the ability to be flexible in varying environmentsAbility 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 environmentsProven 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 issuesGeneral knowledge of scientific literature search and retrievalLimited 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.

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