Technical Content Officer – Medical Devices (12-Month Contract)

ResMed; Kuala Lumpur; Hybrid; MYR 60,000 - 80,000; Full time

Job summary

A leading global medical technology company is seeking a detail-oriented Technical Content Officer in Kuala Lumpur. This 12-month position involves creating and formatting documentation, coordinating translations, and ensuring compliance in a regulated environment. Candidates should have 1–3 years of experience in technical writing or similar roles. The company offers a competitive salary, global exposure, and hybrid work flexibility.

Benefits

Competitive remuneration package

Exposure to a global medical leader

Collaborative culture

Hybrid work flexibility

Qualifications

• 1–3 years of experience in a similar role.
• Experience in a regulated industry (medical devices, pharma).
• Ability to manage multiple tasks within tight timelines.

Responsibilities

• Create and format content in the Enterprise Labelling System.
• Coordinate translations and support technical reviews.
• Maintain and update legacy content for compliance.

Skills

Detail-oriented

Organized

Content entry

Technical writing

Education

Diploma or degree in Life Sciences

Biomedical Engineering

Technical Writing

Communications

Job description

Overview

Are you detail-oriented, organized, and passionate about delivering high-quality documentation in a regulated environment? ResMed is looking for a Technical Content Officer to join our Labelling Centre of Excellence (LCOE) in Kuala Lumpur!

This is a 12-month fixed-term opportunity where you’ll play a key role in ensuring our medical device labelling content is accurate, compliant, and ready to support global healthcare needs.

Role Overview

Let’s Talk About the Role:

As a foundational member of the Labelling team, you’ll be responsible for:

• Creating and formatting content in our Enterprise Labelling System (ELS) using defined templates and standards.

• Coordinating translations and supporting technical review cycles with cross-functional teams.

• Maintaining and updating legacy content to ensure consistency and compliance.

• Tracking progress, meeting deadlines, and escalating blockers when needed.

• Ensuring accuracy and completeness of all entries, with a strong focus on quality.

About You

Let’s Talk About You:

We’re seeking someone who is:

• Experienced in content entry, documentation, or administrative support—ideally in a regulated industry (medical devices, pharma, etc.).

• Detail-oriented with a keen eye for formatting and data accuracy.

• Organized and able to manage multiple tasks within tight timelines.

• A clear communicator who’s eager to learn and grow in a collaborative environment.

Qualifications & Experience

• 1–3 years of experience in a similar role is ideal.

• A diploma or degree in Life Sciences, Biomedical Engineering, Technical Writing, Communications, or related fields is preferred but equivalent experience in regulated documentation or content management is also welcome.

What’s in It for You?

• Competitive remuneration package

• Exposure to a global medical leader in medical technology, improving lives worldwide

• Work with cross-functional teams in a collaborative culture

• Hybrid work flexibility

Ready to Make an Impact?

If you’re passionate about precision, thrive in structured environments, and want to contribute to products that improve lives globally—we’d love to hear from you!

#LI-APAC

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. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.