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Translation Excellence is seeking a Polish Life Science Linguist (Translator, Reviewer, & Editor) to deliver high-quality translations of clinical, regulatory, and medical device documents. The role is project-based, focusing on accuracy, terminology consistency, and regulatory compliance.
Candidates should have 5+ years in life science translation/editing, advanced life sciences or translation education, and strong CAT tool skills (SDl Trados, memoQ, Memsource).
We are seeking a highly specialized Life Science Linguist to provide high-quality translation, revision, and editing services for technical, medical, and regulatory documents. As a 1099 contractor, you will work independently on a project-by-project basis to ensure that complex scientific content is accurately rendered into the target language while maintaining strict compliance with industry standards and regulatory requirements.
Translation: Convert complex life science documents (e.g., clinical trial protocols, ICFs, dossiers, and medical device manuals) from English (USA) to Polish with 100% technical accuracy.
Review & Revision: Conduct bilingual reviews of translated materials against the source text to ensure no omissions, mistranslations, or terminology errors.
Editing & Proofreading: Refine the style, flow, and grammar of target-language content to ensure it is culturally appropriate and meets the "native-level" quality expected for publication or regulatory submission.
Terminology Management: Maintain and update client-specific glossaries and translation memories to ensure consistency across large-scale projects.
QA Compliance: Adhere to ISO 17100 and ISO 13485 standards for linguistic quality and risk management.
Education: Advanced degree (MA, MS, PhD, or MD) in a Life Science discipline (Biology, Chemistry, Pharmacy, etc.) or a degree in Translation with significant field experience.
Experience: 5+ years of professional experience in life science translation/editing.
Linguistic Skill: Native-level fluency in the target language and professional-level mastery of the source language.
Technical Proficiency: Extensive experience with CAT Tools (e.g., SDL Trados, memoQ, Memsource).
Subject Matter Expertise: Proven ability to handle high-stakes regulatory content, such as EMA/FDA filings or MedDRA/EDQM terminology.