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

lilly· 550 Eli Lilly Services India Pvt Ltd
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📍 India, BengaluruFull time

About this role

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

Frequently Asked Questions

Is the salary disclosed for the Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization position at lilly?
The salary for this Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization role at lilly is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization position at lilly located?
This Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization role at lilly is based in India, Bengaluru. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization role at lilly full-time or part-time?
This is listed as a Full time position. It is posted as a Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization role in the 550 Eli Lilly Services India Pvt Ltd department at lilly.
Which team or department does the Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization at lilly belong to?
This Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization position is part of the 550 Eli Lilly Services India Pvt Ltd department at lilly. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization position at lilly?
Click the "Apply Now" button on this page. You will be redirected to lilly's official application portal hosted on workday where you can submit your application directly.
When was the Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization job at lilly posted?
This Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization position at lilly was posted on Sep 26, 2026. Apply as soon as possible — early applications are often reviewed first.
Scientific Writer/Senior Scientific Writer- Quality Review and Document Finalization
lilly
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You'll be redirected to lilly's official application page on Workday.