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Non-Linguistic Quality Control Specialists (US)

See listing · Welo Data · remote

Open to people living in the United States.

Check history

CheckedStatusSlots leftChangeHow
17 Oct 2026Open––Script, platform’s board
15 Oct 2026Open––Script, platform’s board
14 Oct 2026Open––Script, platform’s board
13 Oct 2026Open––Script, platform’s board
12 Oct 2026Open––Script, platform’s board
11 Oct 2026Open––Script, platform’s board
10 Oct 2026Open––Script, platform’s board

The script reads the platform’s own job board every night. A job not confirmed for 10 days comes off the list.

An older role: first posted 72d ago, and Welo Data still listed it when it was last checked on 17 Oct 2026. Newer roles tend to fill faster. See the jobs hiring now.

What the work is

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

About the Role

We are currently looking for freelance professionals to supportNon-Linguistic QC activities for our translation projects in the Life Sciences domain.

Non-Linguistic QC is the final quality assurance step before delivery to the client. Typical tasks include checking for inconsistencies, numeric mismatches, formatting and layout issues, and ensuring client-specific requirements have been followed.

Key Responsibilities

  • 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).

Who gets hired

QC/QA Experience

  • Minimum 6 months QC/QA-related experience in the localization industry. *Project management experience involving pre-delivery checks can also be counted.

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

English Proficiency

  • Advanced level in English (C1 or above)

Availability

  • 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.

Before Applying

Please note there will be an assessment as part of our onboarding and quality procedure, please only apply if you're willing to complete our assessment.

Please ensure your latest English CV accurately reflects your QC related experience, including years of experience, the document types you’ve QCd, CAT tool you've used, and relevant details also your contact information (email AND phone number).

We look forward to receiving your application!

Job Reference: #LI-JC1

The platform posted this on 6 Aug 2026.

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