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We are seeking an Associate Technical Writer to support the development and maintenance of labelling technical content within a regulated medical device environment. This role will operate across both existing (legacy) labelling processes and a new enterprise labelling system (ELS) as the business transitions to future ways of working. The role is ideal for someone early in their career who is detail-oriented, eager to learn, and comfortable working in structured, compliance-driven environments.
Job Responsibility:
Support creation and maintenance of labelling technical documentation
Execute labelling updates using established legacy processes and tools
Create and update content within the Enterprise Labelling System (ELS) under guidance
Perform proofing and quality checks to ensure accuracy, completeness, and compliance to our processes, style guides and brand
Support reviews, approvals, and change management activities
Requirements:
2–3 years of experience in a similar role is ideal
Degree in engineering, science, quality, regulatory, or related discipline (or equivalent experience)
Strong attention to detail and organisational skills
Clear written and verbal communication
Ability to follow defined processes and work under guidance
Willingness to learn in a regulated environment
Nice to have:
Exposure to regulated documentation (medical devices, pharma, or similar)
Familiarity with document or content management systems
Basic understanding of regulatory or quality principles