Job Overview:
Project Role: Content Design Specialist
Work Experience: Fresher
Work location: Thane(Only candidates from thane are preferred)
Work Mode : Hybrid - Night Shift
Must Have Skills: DTP,OCR,Abbyy Finereader ,Illustrator,Indesign,MS office.
Job Description:
We are looking for a meticulous and quality-driven Content Design Specialist to join our CDS team, supporting global life sciences clients.
This role involves handling complex regulatory, clinical, and scientific documentation with a high degree of accuracy and consistency. The specialist will work across OCR, Desktop Publishing (DTP), and Localization workflows to prepare, format, and finalize multilingual content in line with industry standards and client-specific requirements.
Key Responsibilities
OCR- Convert image-based documents (e.g., protocols, brochures, inserts) to editable formats using ABBYY FineReader or similar tools. Perform quality checks and apply proper formatting, structure and language tagging.
DTP- Format localized scientific documents using Adobe InDesign, FrameMaker, MS Word, and PowerPoint. Handle multilingual content layout while ensuring page consistency, proper alignment, and template compliance. Apply regulatory formatting standards.
Localization Support Prepare and clean files for translation, ensuring CAT tool compatibility. Integrate translated content back into the layout while maintaining fidelity to the source. Communicate with PMs and linguists to resolve any formatting or encoding issues.
Skills & Experience We are looking for fresher who can work in OCR/DTP/Localization (preferably in Life Sciences). Strong proficiency in Adobe Creative Suite, Microsoft Office, OCR tools (ABBYY). Familiarity with CAT tools like MemoQ. Excellent attention to detail, layout consistency and formatting compliance.

Keyskills: Good English Communication MS Office DTP Desktop Publishing
IQVIA Biotech provides clinical development services to the pharmaceutical, biotech, and medical device industries. They specialize in supporting smaller biotech firms by offering expertise in clinical trials, regulatory compliance, and drug development.