Medical Device Quality jobs in Melbourne VIC
- Moderna, Inc.Melbourne VIC
- Annual leave
- Sabbatical
- Paid volunteer leave
- Make quality decisions and escalate issues that may impact operations or product quality.
- Strong understanding of cGMP requirements and quality systems.
- Techtronic Industries (TTI)Mount Waverley VIC
- Monitor inspection trends and quality metrics to support quality improvement initiatives.
- Conduct product inspections in line with established quality criteria…
Senior Quality Associate
Often replies in 1 dayContract ManufacturingMelbourne VIC- When required, the role may act as a delegate for the Quality Manager, supporting day-to-day quality activities and ensuring continuity of quality operations.
- KBRMelbourne VIC 3000
- Parental leave
- Insurance services
- Salary packaging
- Complimentary flu shots
- Provide technical authority across quality assurance, audits, inspections, testing, and quality improvement methodologies.
- View all KBR jobs - Melbourne jobs - Quality Manager jobs in Melbourne VIC
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- PSC BiotechMelbourne VIC
- Support vendor qualification and supplier quality activities as required.
- Minimum 4 years of experience in Quality Assurance, Validation, , Manufacturing…
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- Blackmores GroupBraeside VIC
- Drive continuous improvement initiatives that enhance quality, compliance and efficiency.
- Lead quality oversight of tablet, capsule and soft gel manufacturing…
Quality Manager
Often replies in 5 daysMoog Inc.Melbourne VIC- 5+ years’ experience leading and managing quality function in the medical device, aviation, defence and/or automotive field.
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- LivaNovaMelbourne VIC
- Knowledge of medical device regulations and quality systems (ISO 13485, ISO 14971, GMP) is advantageous.
- This role sits within the Engineering Department and…
- Department of Health, Disability and AgeingMelbourne VIC
- Candidates are required to have a high degree of experience in the manufacture and/or quality assurance/quality control of medicines, including extensive…
- The Florey InstituteHeidelberg VIC
- Familiarity with TGA medical device requirements and post-market obligations.
- Background in medical devices, digital health, SaMD, biotechnology or related…
- Moderna, Inc.Melbourne VIC
- Annual leave
- Sabbatical
- Paid volunteer leave
- Coach manufacturing and support teams on validation principles, documentation practices, investigation quality, and risk-based quality expectations to…
- LivaNovaMelbourne VIC
- Assemble medical device set as per drawing instructions to the highest quality of product and compliance to all standards and regulations is achieved in the…
- View all LivaNova jobs - Melbourne jobs
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- LivaNovaMelbourne VIC
- Strong foundational knowledge of mechanical engineering principles applied to medical device packaging systems.
- Tools and Technologies Used in the Role.
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- UGL LimitedSouthbank VIC
- Salary packaging
- Wellness program
- Overseeing the quality control throughout the project life cycle and ensuring we meet the projects objectives and deliverables.
- View all UGL Limited jobs - Southbank jobs
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- UGL LimitedSouthbank VIC
- Salary packaging
- Wellness program
- Overseeing the quality control throughout the project life cycle and ensuring we meet the projects objectives and deliverables.
- View all UGL Limited jobs - Southbank jobs
- Salary Search: Project Manager salaries in Southbank VIC
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- UGL LimitedSouthbank VIC
- Salary packaging
- Wellness program
- The role will also define the project’s objectives and oversee quality control throughout its life cycle.
- We provide end-to-end solutions on major projects…
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Job Post Details
Quality Assurance, On-the-Floor - job post
Job details
Job type
- Full-time
Location
Benefits
Pulled from the full job description
- Annual leave
- Sabbatical
- Paid volunteer leave
Full job description
The Role:
Reporting to the QA Operations Head, MTC-M, the Quality Assurance On-the-Floor Specialist is accountable for providing real-time quality oversight of manufacturing operations at Moderna’s Melbourne site. This role ensures adherence to cGMP requirements and supports both Drug Substance and sterile Drug Product manufacturing through proactive quality engagement.
This role provides end-to-end oversight of on-the-floor quality activities, ensuring compliance with quality systems, regulatory expectations, and operational excellence.
The role supports cross-functional teams including Operations, Manufacturing Science and Technology (MSAT), and Engineering to enable successful and compliant manufacturing outcomes. This position contributes to maintaining a strong quality culture, driving continuous improvement, and ensuring readiness for inspection and validation activities.
Here’s what you’ll do:
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Provide on-the-floor Quality support to Manufacturing (Drug Substance and sterile Drug Product), including real-time observation of activities.
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Monitor process operations to ensure compliance with specifications and regulatory requirements.
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Make quality decisions and escalate issues that may impact operations or product quality.
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Identify risks and communicate gaps in quality systems and GMP processes.
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Perform routine walkthroughs of manufacturing suites to ensure GMP compliance and troubleshoot issues.
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Enforce adherence to cGMPs, SOPs, and manufacturing documentation.
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Partner with manufacturing and support teams to initiate and triage deviation events and review minor deviations.
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Author and review documentation, including SOPs, work instructions, and batch records.
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Ensure safe work practices in line with Moderna procedures and guidelines.
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Support continuous improvement initiatives to enhance operational efficiency.
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Complete required training and maintain qualifications in line with role expectations.
Here’s What You’ll Need (Basic Qualifications)
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Bachelor’s degree in a science-related field (e.g. Biology, Microbiology, Chemistry, Pharmacy, Engineering) or equivalent experience.
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3–5 years of pharmaceutical or related experience in a GMP environment.
Here’s What You’ll Bring to the Table (Preferred Qualifications)
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Experience in sterile drug product manufacturing (preferred).
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Strong understanding of cGMP requirements and quality systems.
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Ability to make independent decisions and escalate issues appropriately.
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Strong cross-functional collaboration and communication skills.
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Attention to detail with a focus on compliance and quality.
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This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.
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As part of Moderna’s commitment to workplace health and safety, this role may be subject to pre-employment and periodic medical assessments, in line with relevant legal and operational requirements.
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.
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Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
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A holistic approach to well-being with access to fitness, mindfulness, and mental health support
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Family building benefits, including fertility, adoption, and surrogacy support
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Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
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Savings and investments to help you plan for the future
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Location-specific perks and extras
The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at leavesandaccommodations@modernatx.com .