Non-Linguistic Quality Control Specialists (US Timezone)
关于韦洛生命科学，威洛全球品牌是专门服务于在监管的全球市场上运营的制药，CRO 和医疗设备组织的语言和技术合作伙伴。我们提供准备好调控器的翻译，语文验证和本地化解决方案，支持临床试验，药物警，监管事务，标签和全球商业化。我们的方法结合了相关专业知识与 ISO 认证质量流程以及旨在无整合到生物科学运作中的技术启用工作流程。凭借支持全球产品开发和市场后需求的丰富经验，Welo Life Sciences 帮助组织加速时间表，保护数据完整性并保持跨语言和地区的合规性。所有解决方案都在7个 ISO 认证所支持的安全，审计准备框架内提供.welolifesciences.com 关于角色 我们目前正在寻找自由职业人士来支持我们的非语文质量检测项目在生命科学领域中的翻译活动。非语文質量检测是向客户交付前最后的质量保证步骤。典型任务包括检查不一致性，数量失调，格式化和布局问题以及确保客户特定要求得到遵守。关键责任 · 对药物监督，监管和临床内容进行非语言质量控制的英语翻译。· 使用 CAT 工具并执行 QC 检查以确保准确性和一致性。·验证格式化，数字，日期，单位，术语和遵循说明。·支持处理不可编辑/手写来源并进行转换后格式化 QC. ·根据可用性工作并满足 TAT （通常1224小时）.要求 QC/QA 经验 · 地方化行业至少6个月的 QC/QA 相关经验。*还可计数项目管理经验，包括预交检查。技术技能 · 与 CAT 工具 (XTM/Phrase) 的熟悉性，许可证将提供。· QA 检查工具 （Xbench, Verifika 或 CAT 集成的 QA）的熟练性 · Microsoft Word 英语变化的熟悉性 · 高级英语水平 （C1以上）可用性 · 每天45小时可用性 · 有灵活性和愿意工作周末和银行假期。·能够满足偶尔紧急 TAT （1224节）.
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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 support Non-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).
Requirements
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