Technical Writer

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Job description

Working with key stakeholders to produce clinical & regulatory documents for IVD product submission.

Your new company
In this role, you will be joining the R&D team of a continually growing business. The company specialises in IVD devices as well as testing equipment for the food and industrial space. The company itself is a fast-paced business and with many sister companies, you are ensured continued growth and progression down many paths within the medical device space.

Your new role

* Conducting in-depth research, and working closely with key stakeholders (product management, regulatory, sales and research & development, etc.);
* Writing high quality technical documentation for submission to Clinical or Regulatory Authorities;
* Developing and maintaining SOPs for the technical writing function in the R&D department;
* Designing content structure, developing content, delivering publication-ready files and maintain documentation;
* Coordinating timely development, change and approval of materials.

What you'll need to succeed

* Tertiary Qualifications in Science, equivalent, or relevant working experience;
* Excellent written, oral, and listening communication skills;
* Technical writing experience in the medical device\/diagnostics\/biomedical industry or equivalent;
* Experience developing technical documents for CE IVD point-of-care diagnostics systems or in writing clinical documents such as Clinical Protocols\/reports.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact Sandy Vo on for a confidential discussion on your career.