Overview

Have you ever read a translated document and instantly spotted that one tiny typo everyone else glossed over? At Welo Life Sciences, we live for that exact level of detail. We are currently growing our non-linguistic quality control team and we need sharp minds who treat precision as an art form. If you want your daily work to directly protect patient safety in the pharmaceutical and medical device sectors, this fully remote opportunity across Europe is tailor-made for you.

Key Responsibilities

Review translated documents meticulously to ensure flawless English grammar, formatting, and overall visual presentation.
Execute rigorous quality control checks specifically tailored for pharmacovigilance, regulatory affairs, and clinical trial materials.
Catch layout shifts, punctuation errors, and inconsistencies that automated spelling tools always seem to miss.
Collaborate seamlessly with project managers and translation teams to uphold the highest regulatory compliance standards.

Requirements

Proven professional experience handling clinical or regulatory documents such as medical reports, study protocols, synopses, informed consent forms, and patient information leaflets.
Exceptional attention to detail with a natural inclination toward spotting subtle errors in complex texts.
Native or near-native English proficiency combined with a strong analytical mindset.
Reliable high-speed internet connection and a quiet home office setup for remote work.

What You'll Gain

Consistent, daily project volume giving you steady work and predictable scheduling.
Long term career growth potential within a high visibility program serving world leading pharmaceutical and contract research organizations.
The satisfaction of knowing your meticulous eye for detail genuinely impacts global healthcare outcomes.