Technical Writer - Medical Devices (12-month Contract)
mementor DE GmbH
Labelling technical documentation creation
Experience in regulated medical device environment
Attention to detail and organisational skills
At ResMed, we are committed to transforming our Medical Device labelling capabilities to ensure compliance with the evolving regulatory regulations worldwide
Job Summary
At ResMed, we are committed to transforming our Medical Device labelling capabilities to ensure compliance with the evolving regulatory regulations worldwide.
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.
Joining us is more than saying “yes” to making the world a healthier place; it’s discovering a career that’s challenging, supportive and inspiring.
Matching Summary
At ResMed, we are committed to transforming our Medical Device labelling capabilities to ensure compliance with the evolving regulatory regulations worldwide.
Skills & Requirements
Must-have
Labelling technical documentation creation
Experience in regulated medical device environment
Attention to detail and organisational skills
Working with legacy and enterprise labelling systems
Proofing and quality checks for compliance
Nice-to-have
Exposure to regulated documentation
Familiarity with content management systems
Understanding of regulatory or quality principles
Eager to learn in compliance-driven environments
Comfortable working under guidance
Key Requirements
2–3 years experience in similar role
Degree in engineering, science, quality, regulatory or related discipline