About Welo Life Sciences 

Welo Life Sciences, a Welo Global brand, is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations operating in regulated global markets. We deliver regulator-ready translation, linguistic validation, and localization solutions that support clinical trials, pharmacovigilance, regulatory affairs, labeling, and global commercialization. Our approach combines subject matter expertise with ISO-certified quality processes and technology-enabled workflows designed to integrate seamlessly into life sciences operations. With extensive experience supporting global product development and post-market requirements, Welo Life Sciences helps organizations accelerate timelines, protect data integrity, and maintain compliance across languages and regions. All solutions are delivered within a secure, audit-ready framework supported by seven ISO certifications. welolifesciences.com

• Perform Non-Linguistic Quality Control of translations into English for pharmacovigilance, regulatory, and clinical content.
• Use CAT tools and run QC checks to ensure accuracy and consistency.
• Validate formatting, numbers, dates, units, terminology, and adherence to instructions.
• Support processing of non-editable/handwritten sources and perform formatting QC after conversion.
• Work according to availability and meet TATs (typically 12–24 hours).
  

Technical Skills

• Familiarity with CAT tools (XTM/Phrase), License will be provided.
• Familiarity with QA checks tools (Xbench, Verifika, or CAT-integrated QA)
• Familiarity with Track Changes in Microsoft Word

• Advanced level in English (C1 or above)

• Availability of 4–5 hours per day
• Flexibility and willingness to work occasional weekends and bank holidays.
  
• Able to meet urgent TATs (12–24 hours) and manage many small files.