In-Demand Regulatory affairs specialist Jobs in Bella Vista, Nsw

Labelling Systems Specialist (12-Month Contract)
ResMed —Bella Vista NSW
- Full-time
- AI
- Communication skills
Technical Sales Rep - Pharmaceutical Product Specialist
Sci-Chem International Pty Ltd —Prestons NSW
- $83,000 - $90,000 a year
- Full-time
- Management
- Sales
- Bachelor's degree
Quick Apply
Senior Marketing Specialist
Solventum —North Ryde NSW
- Full-time
- Sales
- Marketing
- Organisational skills

Related jobs to explore

Based on your search for regulatory affairs specialist

Research Strategist
Avant —Sydney NSW
Tertiary qualifications at bachelor's or master's level (discipline agnostic). Experience with health and medical research, and insight into the Australian…
$250,000 a year
Labelling Systems Specialist (12-Month Contract)
ResMed —Bella Vista NSW
We are seeking a Labelling Systems Specialist to support the development and evolution of labelling content within a regulated medical device environment.

I want to receive the latest job alert for regulatory affairs specialist in bella vista, nsw

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs specialist jobs near bella vista, nsw

Senior Marketing Specialist jobs in Melbourne Vic

Senior Marketing Specialist jobs in Byron Bay Nsw

Senior Director Public Policy Apac jobs in Sydney Nsw

Senior Marketing Specialist jobs in Chadstone Vic

Senior Marketing Specialist jobs in Ashmore Qld

Senior Citizens jobs in Milperra Nsw

Senior It System Administrator jobs in Melbourne Vic

Marketing Coordinator jobs in Maidstone Vic

Regulatory Affairs Specialist jobs in Milsons Point Nsw

Aboriginal Director Aboriginal Affairs jobs in Sydney Nsw

Regulatory Affairs Specialist jobs in Sydney Nsw

Melbourne Veterinary Specialist Centre jobs in Glen Waverley Vic

Regulatory Affairs Manager jobs in Sydney Nsw

Labelling Systems Specialist (12-Month Contract)

ResMed -
Bella Vista NSW

Apply Now

Job Details

Full-time

Qualifications

AI
Document management systems
Communication skills

Full Job Description

At ResMed, we are committed to transforming our Medical Device labelling capabilities to ensure compliance with the evolving regulatory regulations worldwide. This transformation is crucial for maintaining the highest standards in our industry.

About the Role

We are seeking a Labelling Systems Specialist to support the development and evolution of labelling content within a regulated medical device environment.

This role sits at the intersection of systems, regulatory, and product development, contributing to both the optimisation of existing labelling processes and the transition to our Enterprise Labelling System (ELS).

You will bring a systems-thinking mindset, strong communication skills, and a continuous improvement approach to how content is created, structured, and managed — including exploring the use of AI and emerging technologies to enhance efficiency, scalability, and quality.

Key Responsibilities

Develop, maintain, and manage labelling content across legacy platforms and enterprise systems
Translate regulatory, engineering, and product requirements into clear, accurate, and compliant documentation
Contribute to content creation, structuring, and governance within the Enterprise Labelling System (ELS), supporting adoption of new ways of working
Ensure accuracy, consistency, and traceability of labelling artefacts in alignment with regulatory and quality standards
Collaborate cross-functionally with Regulatory Affairs, Quality, Systems Engineering, and Product teams
Support continuous improvement initiatives, including process optimisation and digital/AI-enabled solutions
Participate in content reviews, approvals, and change management processes

Skills & Experience

Essential

Experience in technical writing, regulatory, quality, or engineering roles within a regulated environment
Excellent written and verbal communication skills, with the ability to translate complex information into clear, user-friendly content
Proven ability to collaborate effectively across multiple stakeholders and functions
Strong attention to detail with a solid understanding of compliance-driven environments

Desirable

Experience within the medical device industry or similar highly regulated sectors
Exposure to design controls, product development processes, or structured technical documentation
Familiarity with document management systems or structured content/authoring platforms
Interest or exposure to AI, automation, or digital content solutions

Who You Are

A proactive and self-motivated learner who takes initiative
Curious, with a continuous improvement mindset toward systems and processes
Comfortable working in structured, regulated environments
A strong communicator who can engage and influence diverse stakeholders

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. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. 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.

Apply Now

Refine Your Search

regulatory affairs specialist jobs in bella vista, nsw

Labelling Systems Specialist (12-Month Contract)

Technical Sales Rep - Pharmaceutical Product Specialist

Senior Marketing Specialist

Related jobs to explore

I want to receive the latest job alert for regulatory affairs specialist in bella vista, nsw

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected