In-Demand medical device regulatory Jobs in sydney nsw

Medical Writer ANZ
Zimmer Biomet —Sydney NSW
- Full-time
- Management
- Doctoral degree
- Microsoft Office
- Wellness program
Product Manager - Medical Devices
BD —North Ryde NSW
- Contract
- Management
- Product management
- Communication skills
Regulatory Affairs Associate
PharmaCare Group —Warriewood NSW
- Full-time
- Analysis skills
- Communication skills
Quick Apply
8d
Regulatory Affairs Manager
BD —North Ryde NSW
- Contract
- Maintenance
- Master's degree
- Bachelor's degree
- Parental leave
Specialist, Clinical Research (12 months contract)
Edwards Lifesciences —North Ryde NSW
- Full-time
- Management
- Patient monitoring
- Microsoft Office
Quality Assurance Specialist
Device Technologies Australia —Sydney NSW
- Full-time
- Communication skills
Senior Regulatory Affairs Specialist
Fresenius Medical Care —North Sydney NSW
- Full-time
- Management
- Engineering
- ERP systems
Research & Development Engineer
Cochlear Limited —Sydney NSW
- $53.12 - $65.14 an hour
- Full-time
- AutoCAD
- Doctoral degree
- CAD
- Health insurance
- Life insurance
Quick Apply
Senior Regulatory Affairs Manager
Galderma —North Sydney NSW
- Hybrid work
- Master's degree
- Bachelor's degree
- Leadership
- Parental leave
Senior Manager, Regulatory Affairs
Cencora —North Sydney NSW
- Full-time
- Hybrid work
- Master's degree
- Education
- Bachelor's degree
QC Specialist
CAI —Sydney NSW
- Contract
- Laboratory experience
- AI
Quick Apply
Study Site Management Specialist
Smith & Nephew —Sydney NSW
- Full-time
- Hybrid work
- Bachelor's degree
- Annual leave
8d
QA Specialist
CAI —Sydney NSW
- Contract
- Management
- Engineering
- Analysis skills
Quick Apply
Pharmacovigilance Project Manager (Japanese fluency required)
PrimeVigilance —Sydney NSW
- Full-time
- Leadership
Quick Apply
9d
Post Market Quality Assurance Reporting Specialist
AbbVie —Sydney NSW
- Full-time
- Hybrid work
- Clinic
- Bachelor's degree
- Communication skills
2d
Post Market Vigilance Lead
Device Technologies Australia —Sydney NSW
- Full-time
- Communication skills
Clinical Evaluation Manager
Cochlear Ltd —Sydney NSW
- Full-time
- Medicine
- Writing skills
- Leadership
2d
Regional Senior Scientific Affairs Associate
PharmaCare Group —Warriewood NSW
- Full-time
- Research
- Office
- Analysis skills
Quick Apply
3d
Compliance Engineer
ResMed —Sydney NSW
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
Principal System Engineer, Application
Cochlear Ltd —Sydney NSW
- Full-time
- Leadership
- Communication skills

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Medical Writer ANZ

Zimmer Biomet -
Sydney NSW

Apply Now

Job Details

Full-time

Benefits

Wellness program

Qualifications

Management
Doctoral degree
Microsoft Office
Diagnostic evaluation
Master's degree
Bachelor's degree
Organisational skills
Pharmacy
Medical terminology
Communication skills

Full Job Description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

About the Role

We’re looking for an experienced Medical Writer to join our ANZ team and play a key role in shaping high-quality scientific and regulatory content. In this role, you will lead the development of Clinical Evaluation Reports (CERs) to support regulatory submissions for orthopaedic devices and technologies across Australia and New Zealand. You will also prepare and manage post-market surveillance documents and contribute to a range of scientific publications, including journal manuscripts, conference abstracts and white papers.

This role is ideal for someone who thrives on scientific communication, enjoys working across cross-functional teams, and is confident in translating complex clinical data into clear, accurate and engaging content for both internal and external audiences.

Key Responsibilities

Develop and maintain Clinical Evaluation Reports (CERs) in line with TGA requirements, EU MDR (2017/745) and Zimmer Biomet internal standards, drawing on clinical research, peer-reviewed literature, risk management files and post-market data.
Conduct structured literature reviews to support post-market surveillance (PMS) reports.
Prepare scientifically robust responses to regulatory queries, ensuring accuracy and alignment with regional and global standards.
Circulate final draft reports for review and approval across Clinical Affairs, Regulatory Affairs, Post-Market Surveillance and Engineering teams.
Support audit activities and serve as a subject matter expert (SME) as required.
Explore and adopt innovative medical writing approaches, including the use of advanced writing tools and AI, to improve efficiency and output.
Develop, write and edit manuscripts for peer-reviewed journals, ensuring clarity, scientific integrity and adherence to journal guidelines.
Create conference abstracts, posters and presentation materials in collaboration with internal experts.
Prepare white papers, technical summaries and evidence-based narratives to support product value messaging and thought leadership.
Collaborate with Clinical Affairs, Regulatory, R&D and Marketing teams to gather insights, ensure accuracy and support strategic communication initiatives.
Manage multiple projects, deadlines and submission workflows simultaneously.
Support publication planning and broader scientific communication strategies.

What We’re Looking For

Qualifications & Experience

Bachelor’s degree in a scientific, medical or health-related discipline (e.g., life sciences, biomedical engineering).
Postgraduate qualifications (MSc, PhD, PharmD) preffered
Minimum 3 years’ experience in medical writing, ideally within the medical device, pharmaceutical or healthcare sectors.
Demonstrated experience producing manuscripts, abstracts or white papers for scientific or clinical audiences.

Skills & Competencies

Strong understanding of medical device regulatory requirements, including TGA and EU MDR.
Solid knowledge of clinical research methodologies and medical terminology.
Ability to critically evaluate and interpret clinical data.
Familiarity with publication processes, journal requirements and best practice guidelines (e.g., ICMJE, GPP).
Excellent written, editorial and verbal communication skills.
Ability to work independently while contributing effectively within cross-functional teams.
Strong organisational skills with the ability to manage competing deadlines.
Proficiency with Microsoft Office and reference management tools such as EndNote.

EOE/M/F/Vet/Disability

Apply Now

Refine Your Search

medical device regulatory jobs in sydney nsw

Medical Writer ANZ

Product Manager - Medical Devices

Regulatory Affairs Associate

Regulatory Affairs Manager

Specialist, Clinical Research (12 months contract)

Quality Assurance Specialist

Senior Regulatory Affairs Specialist

Research & Development Engineer

Senior Regulatory Affairs Manager

Senior Manager, Regulatory Affairs

QC Specialist

Study Site Management Specialist

QA Specialist

Pharmacovigilance Project Manager (Japanese fluency required)

Post Market Quality Assurance Reporting Specialist

Post Market Vigilance Lead

Clinical Evaluation Manager

Regional Senior Scientific Affairs Associate

Compliance Engineer

Principal System Engineer, Application

I want to receive the latest job alert for medical device regulatory in sydney nsw

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