Welo Global
Non-Linguistic Quality Control Specialists (Europe)
EURemotePosted Today
Full TimeRemoteEU
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Job Description
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 delive
Key Highlights
- Perform Quality Control of translations into English for pharmacovigilance, regulatory, and clinical content.
- Ideal candidate brings experience with clinical/regulatory documents (medical reports, protocols, synopses, ICF, discharge and study reports, SmPC, PIL, medical literature, linguistic validation) or pharmacovigilance documents (SAE/AE, PSURs, SUSARs, ICSRs, DSUR, RMP)
- Use CAT tools (XTM preferred) 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.
Qualifications
Required Qualifications
- Mandatory experience with CAT tools: XTM, Trados, MemoQ, Phrase or others.
- Experience with QA checks: Xbench, Verifika, or CAT-integrated QA.
- Experience with Track Changes function in Word.
- Minimum 6 months as a Language QA specialist in localization.
- Advanced English level, min. C1
- Availability of 4–5 hours per day; willing to work weekends and bank holidays.
- Able to meet urgent TATs (12–24 hours) and manage many small files.
- Willing to complete the QC test and follow staged onboarding.
- Prior experience with a similar QC role at an LSP is a strong plus.
- Flexibility and willingness to work occasional weekends and bank holidays.
Preferred Qualifications
- Flexibility and willingness to work occasional weekends and bank holidays.
About the Company
Welo Global
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Job Details
Employment Type
Full Time
Location
EU
Work Mode
Remote
Posted
Today
Country
EU