英语到法语加拿大版（药物警戒语言学家）
English to French Canadian for Pharmacovigilance Linguist
关于 Welo Life Sciences
Welo Life Sciences 是 Welo Global 品牌，是一家专注于语言和技术的合作伙伴，为在受监管全球市场运营的制药公司、CRO 和医疗设备组织提供服务。我们提供符合监管要求的翻译、语言验证和本地化解决方案，支持临床试验、药物警戒、法规事务、标签和全球商业化。我们的方法结合了专业领域知识与 ISO 认证的质量流程和技术驱动的工作流，旨在无缝集成到生命科学运营中。凭借丰富的全球产品开发和上市后要求支持经验，Welo Life Sciences 帮助组织加快时间表、保护数据完整性，并在多种语言和地区保持合规性。所有解决方案均在安全、可审计的框架内交付，该框架由七项 ISO 认证支持。 welolifesciences.com
我们正在寻找有经验且技能娴熟的英语到加拿大法语语言学家加入我们专注于药物警戒的生命科学项目。这是一个令人兴奋的机会，参与关键的医学和临床内容，为全球健康和安全计划做出贡献。
在此职位中，您将发挥关键作用，确保在紧迫的截止日期内准确及时地交付翻译。许多任务具有时间敏感性，需要快速完成以满足客户期望，同时保持最高质量标准。
加入我们的全球团队，通过交付高质量的翻译来推动全球健康，支持关键的医学研究和患者安全。
职位编号：#LI-JC1
职位关键信息
- 将英文（美国）文档翻译成法文（加拿大），重点在于药物警戒相关内容。
- 根据需要执行翻译、校对（CE）和机器翻译后期编辑（MTPE）任务，确保高质量标准和一致性。
- 翻译专业医学和制药内容，包括药品说明书、临床研究文件和医学信息信函。
- 遵守严格的截止日期，特别是针对欧盟工作时间结束时收到的项目，需在清晨交付。
- 在客户提供的 XTM 和 Phrase（Memsource）CAT 工具中工作（将提供许可证）。
- 保持专业性、响应性和可靠性，以满足客户期望。
查看英文原文
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
We are currently seeking experienced and highly skilled English to Canadian French linguists to join our dynamic Life Sciences program specializing in Pharmacovigilance. This is an exciting opportunity to work on vital medical and clinical content, contributing to global health and safety initiatives.
In this role, you will play a critical part in ensuring the accurate and timely delivery of translations under tight deadlines. Many assignments are time-sensitive, requiring quick turnarounds to meet client expectations while maintaining the highest standards of quality.
Join our global team and help us make a difference in global health by delivering high-quality translations that support critical medical research and patient safety.
Job Reference: #LI-JC1
Key Details About the Role
- Translate documents from English (US) to French (Canada), with a focus on pharmacovigilance content.
- Perform Translation, Copy Editing (CE), and Machine Translation Post Editing (MTPE) tasks as required, ensuring high-quality standards and consistency.
- Translate specialized medical and pharmaceutical content, including Product Monographs, Clinical Study Documents, and Medical Information Letters.
- Adhere to tight deadlines, especially for projects received during EU close-of-business hours, with delivery required for early morning.
- Work within the client-provided XTM and Phrase (Memsource) CAT tools (licenses will be provided).
- Maintain professionalism, responsiveness, and reliability to meet client expectations and ensure timely delivery of assignments.
Requirements
- Proven experience in medical and pharmaceutical translation, particularly for pharmaceutical companies or life sciences translation agencies in Quebec or Canada.
- Specific expertise in translating Product Monographs and Medical Information Letters.
- Bachelor’s degree in translation or a bachelor’s degree in science (e.g., pharmacology, biology, biochemistry) combined with a translation degree from a Quebec or Canadian university.
- Membership in a Professional Order (e.g., OTTIAQ) is highly preferred.
- Fluency in English (source language) and native-level proficiency in French (Canada) (target language).
- Availability during US time zone business hours (location can be any country).
- Strong attention to detail, consistency, and commitment to meeting deadlines under time-sensitive conditions.
- Familiarity with CAT tools, specifically XTM and Phrase (Memsource) (training provided if necessary).
- Ability to handle sensitive and technical content with confidentiality and precision.
Bonus if You Have
- Experience working with high-volume, time-critical translation projects.
- Strong background in pharmacovigilance, medical, or pharmaceutical content.
- Previous experience working in collaborative environments with strict client guidelines.
- Positive track record of professionalism and reliability in previous roles.