Indiranagar Bengaluru Karnataka Technical document writer Jobs – 54 Open Jobs Today

Scientific Writer • Global Scientific Communications Toxicology Non-clinical submissions
Lilly —Bengaluru, Karnataka
- Full-time
- Project management
15h
Desktop Technical Publication
UST Global —Bengaluru, Karnataka
- Microsoft Powerpoint
- Microsoft Outlook
- English
Technical Writer
MASTER MIND CONSULTANCY —Bengaluru, Karnataka
- ₹27 an hour
- Microsoft Powerpoint
- Microsoft Word
- Engineering
Quick apply
Technical Publications Associate
Newspace —Bengaluru, Karnataka
- Bachelor's degree
- Communication skills
Quick apply
Technical Writer – Warehouse Automation / WMS Domain
Quest Global —Bengaluru, Karnataka
- Full-time
- Microsoft Office
- APIs
- Communication skills
Quick apply
TECHNICAL WRITER INTERN
Jivox —Bengaluru, Karnataka
- Email
- Microsoft Powerpoint
- English
- Research
Sr Safety Medical Writer
Novo Nordisk —Bengaluru, Karnataka
- Doctoral degree
- English
- Master's degree
Content Writer
Garuda Aerospace —Bengaluru, Karnataka
- Writing skills
- English
- Editing
IND Analyst II - Proposal Management
Aon Corporation —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- English
- Commuter assistance
Proposal Coordinator
GE Vernova —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
12h
1700_SR Medical Writer
Recruise —Bengaluru, Karnataka
- Full-time
- Project management
- Time management
Quick apply
Senior Medical Writer
CELEGENCE —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
SEO Analyst / Expert
EMS Web Designing Company —Bengaluru, Karnataka
- Master's degree
- Bachelor's degree
- Scripting
Content Development Specialist
Accenture —Bengaluru, Karnataka
- Full-time
- Google Suite
- English
- Communication skills
Technical Content Strategist
Automation Anywhere —Bengaluru, Karnataka
- Email
- Quality control
- AI
- Analytics
Content Developer, Customer Trust Content Management
ADCI - BLR 14 SEZ —Bengaluru, Karnataka
- Full-time
- English
- Bachelor's degree
- Organizational skills
Lead Medical Writer
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- Master's degree
4d
Content Developer, Risk Content Management
ADCI - BLR 14 SEZ —Bengaluru, Karnataka
- Full-time
- English
- Bachelor's degree
- Organizational skills
Senior Medical Writer
Navitas Life Sciences —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Medicine
SAP ABAP Consultant
Aexonic Technologies —Bengaluru, Karnataka
- Email
- Hybrid work
- Computer Science
- Analysis skills
- Bachelor's degree

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Scientific Writer • Global Scientific Communications Toxicology Non-clinical submissions

Lilly -
Bengaluru, Karnataka

Apply Now

Job details

Full-time
15 hours ago

Qualifications

Project management

Full job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Purpose:

Scientific data and information are Lilly's core assets. It is fundamental to Lilly to consistently and timely provide balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients throughout the entire drug development lifecycle.

The purpose of the Associate- Toxicology/ Non-Clinical Submissions role is to work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences (including, but not limited to, nonclinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and Marketing Authorization Applications).

Primary Responsibilities:

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position can change over time and can include additional responsibilities not specifically described in the job description.

Document Preparation, Development and Finalization/Document Management

Plan (including organizing/preparing outlines), write (including transferring data and authoring in a templated report format), edit, review, coordinate, and complete the ADME study reports supporting nonclinical development/product registration.
Ensure data are presented in a clear, complete, accurate, and concise manner
Conduct effective submission/document initiation meetings to ensure nonclinical team alignment and understanding
Ensure that key data, statements and conclusions are consistent across all related nonclinical documents
Format/Publish nonclinical deliverables as per regulatory standards

Project and Stakeholder management

Lead the submission process and apply effective project management skills to ensure timely completion of high-quality regulatory documents
Build/communicate credible writing/submission project timelines for the nonclinical team
Ensure and coordinate authoring, peer/management/ regulatory reviews, quality checks for accuracy
Effectively coordinate submission activities with Absorption/Distribution/Metabolism/Excretion (ADME), Toxicology (Tox)/ Pathology (Path), Pharmacokinetics (PK)/Pharmacodynamics (PD) (ATP) scientists, discovery biologists, and environmental risk assessment scientists
Anticipate and mitigate risks, to ensure document completion and delivery
Effectively communicate project status to stakeholders
Exhibit flexibility in coordinating preparation of multiple document types

Nonclinical Submissions Coordination

Establish and manage nonclinical regulatory submission timing and deliverables
Serve as the subject matter expert for nonclinical electronic Common Technical Document (eCTD) content, as well as for nonclinical document and submissions planning
Track progress, including document publishing, approval, and transition, to the regulatory submission publishing team

Knowledge Sharing and Skills Development

Maintain and enhance knowledge of regulatory guidelines
Provide guidance to others regarding any nonclinical submission/documents related information
Recognized for technical expertise in specific document development
Network with others (including other functions and regions) to identify and share best practices
Contribute to process improvements, suggesting opportunities where appropriate
Perform other duties as assigned by management

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

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Refine Your Search

technical document writer jobs in indiranagar bengaluru karnataka

Scientific Writer • Global Scientific Communications Toxicology Non-clinical submissions

Desktop Technical Publication

Technical Writer

Technical Publications Associate

Technical Writer – Warehouse Automation / WMS Domain

TECHNICAL WRITER INTERN

Sr Safety Medical Writer

Content Writer

IND Analyst II - Proposal Management

Proposal Coordinator

1700_SR Medical Writer

Senior Medical Writer

SEO Analyst / Expert

Content Development Specialist

Technical Content Strategist

Content Developer, Customer Trust Content Management

Lead Medical Writer

Content Developer, Risk Content Management

Senior Medical Writer

SAP ABAP Consultant

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