English to Spanish (ESMX native) for Life Sciences Linguist

Jobgether SRL; Netherlands; On-site; EUR 42,000 - 65,000; Full time

Benefits offered by this job

CAT tool licenses

Structured onboarding

Flexible language-focused environment

Exposure to regulated life sciences

Job summary

Lever, Inc. in the Netherlands seeks an English to Spanish (ESMX) Life Sciences Linguist based in the Netherlands.

The role focuses on translating clinical, pharmacovigilance, and regulatory documents from English into native Mexican Spanish to support clinical research and regulatory submissions. You will work with CAT tools such as XTM or Phrase, perform MTPE, and ensure consistency and quality under strict deadlines.

Qualifications

• Strong attention to detail for regulated medical content.
• Ability to meet strict, non-extendable deadlines.
• Experience with life sciences translation including clinical, pharmacovigilance, and regulatory documents.

Responsibilities

• Translate clinical research, pharmacovigilance, regulatory, and medical documents from English into Latin American Spanish (Mexican Spanish).
• Translate patient-facing materials and regulatory submissions.
• Perform MTPE and linguistic review to ensure accuracy and regulatory compliance.
• Work within CAT tool environments (XTM/Phase) and use Word Track Changes per instructions.

Skills

Attention to detail

Deadline-driven

Independent worker

Life sciences translation

Education

Translation / Linguistics degree

Medicine/Biology related degree a plus

Tools

XTM

Phrase

Word Track Changes

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a English to Spanish (ESMX native) for Life Sciences Linguist based in Netherlands.

This role is ideal for an experienced linguist specializing in regulated life sciences content.

You will translate critical clinical, pharmacovigilance, and regulatory documents from English into native Mexican Spanish.

Your work will directly support clinical research, patient-facing materials, drug safety, regulatory submissions, and product labeling.

You will also contribute through machine translation post-editing and detailed linguistic review to ensure accuracy, consistency, and appropriate tone.

The position requires strong attention to detail and the ability to deliver high-quality work within strict, non-extendable deadlines.

You will work within established technology-enabled workflows and client-specific CAT tool environments in a quality-focused setting.

This is an opportunity to apply your language expertise to documents where linguistic accuracy and regulatory compliance are essential.

Accountabilities

• Translate clinical research, pharmacovigilance, regulatory, and medical documents from English into Latin American Spanish, specifically native Mexican Spanish.




• Work across clinical documents such as protocols, synopses, Investigator’s Brochures, Informed Consent Forms, patient sheets, and patient diaries.




• Translate regulatory materials including SmPCs, PILs, labels, and CTD modules.




• Translate pharmacovigilance documentation such as PSURs, DSURs, Risk Management Plans, and SAE/AE content.




• Perform Machine Translation Post-Editing (MTPE) on machine-translated safety and life sciences content.




• Conduct copy editing and linguistic review to ensure accuracy, consistency, tone, terminology, and overall quality.




• Meet strict, non-extendable turnaround times for time-sensitive projects.




• Work within client CAT tool environments such as XTM or Phrase, with licenses provided where applicable.




• Use Microsoft Word Track Changes according to project-specific instructions and workflows.




• Complete a required assessment as part of the onboarding and quality assurance process.

Requirements:

• Native-level Mexican Spanish (ESMX) language proficiency is required.




• At least two years of practical translation experience specifically covering life sciences, clinical trials, pharmacovigilance, and medical documentation.




• A degree in Translation, Linguistics, Language Studies, or an equivalent discipline; alternatively, a recognized graduate qualification in another field combined with at least two years of full-time professional translation experience.




• Candidates may also qualify through a minimum of five years of full-time professional translation experience.




• Familiarity with CAT tools such as XTM or Phrase.




• Proficiency with Microsoft Word Track Changes.




• Strong understanding of terminology, accuracy, consistency, and quality requirements for regulated medical and life sciences content.




• Excellent attention to detail and the ability to work independently against demanding deadlines.




• A degree in Medicine, Biology, Biochemistry, Clinical Research, Translation, Linguistics, Philology, or a related field is a plus.




• Previous in-house experience within a CRO or pharmaceutical organization is advantageous.




• Applicants should ensure their latest English CV clearly reflects their life sciences and medical translation experience, including years of relevant experience, document types handled, CAT tools used, and complete contact information.

Benefits:

• Opportunity to work on specialized clinical, pharmacovigilance, regulatory, and medical content.




• Exposure to a broad range of life sciences documentation and regulated-market workflows.




• Access to CAT tool licenses where required.




• Structured onboarding and quality procedures designed to support high-quality linguistic delivery.




• Opportunity to contribute to projects supporting clinical research, drug safety, regulatory activities, and global commercialization.




• Flexible language-focused work environment centered on specialized translation expertise.




• Opportunity to build further experience in the life sciences translation sector.




• Compensation and additional employment terms are not specified in the provided job description.