Non-Linguistic Quality Control Specialist – Latam

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Logo of Welo Global

Welo Global

1001 - 5000 employees

🤖 Artificial Intelligence

🤝 B2B

☁️ SaaS

Artificial Intelligence • B2B • SaaS

Welo Global is a multilingual content, data, and AI solutions company that provides enterprise-focused localization, regulated translation, and AI training data through a family of brands (including Welocalize, Park IP, Welo Life Sciences, Welo Data, and Adapt). It combines domain expertise, proprietary AI tools (e. g. , the Opal suite), governed global workforces, and compliance certifications to support use cases across global marketing, intellectual property and legal translations, life sciences regulatory and clinical documentation, and AI model development. The company emphasizes scalable, AI-enabled platforms and workflows to deliver high-quality multilingual content and structured datasets in 300+ languages for corporate clients.

📋 Description

• Perform quality control of translations into English for pharmacovigilance, regulatory, and clinical content • Review clinical/regulatory and pharmacovigilance documents for quality • 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 • Self-assign work via Open Offers according to availability and meet urgent turnaround times • Handle high-volume work split across multiple small files; document and report discrepancies • Collaborate with project managers and escalate risks promptly

🎯 Requirements

• Mandatory experience with CAT tools: XTM, Trados, MemoQ, Phrase, or others • Experience with QA checks using Xbench, Verifika, or CAT-integrated QA • Experience with Track Changes in Word • Minimum 6 months as a Language QA specialist in localization • Advanced English level, minimum C1 • Availability of 4–5 hours per day • Willingness to work weekends and bank holidays • Ability to meet urgent 12–24-hour turnaround times and manage many small files • Willingness to complete the QC test and follow staged onboarding • Prior experience with a similar QC role at an LSP is a strong plus • Experience with clinical/regulatory or pharmacovigilance documents is ideal

🏖️ Benefits

• Steady, daily volume and long-term growth potential • Flexibility and willingness to work occasional weekends and bank holidays

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