Analyst, Quality Control, Bioassay

The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.

As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives.

Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide.

Moderna is committed to enhancing Australia's biotech landscape through a long-term partnership that focuses on strengthening pandemic resilience. Our Melbourne-based large-scale mRNA vaccine manufacturing facility will be a cornerstone in Australia's ability to respond to future health threats efficiently. This collaboration not only brings cutting-edge medical technology to the forefront but also emphasizes job creation and local talent development. We're inviting visionary professionals to be part of this transformative journey, making a tangible impact on global health security.

You will be instrumental in supporting Moderna’s growing manufacturing footprint by performing advanced Bioassay Quality Control testing in a GMP setting. Working as part of a dynamic Quality Control team, this position is focused on ensuring the integrity of drug substance and product quality through hands-on molecular biology and protein analytics. The role includes method execution, troubleshooting, and continuous improvement initiatives — all within a high-impact, fast-paced biotech environment. As an individual contributor based at our Clayton site, you’ll collaborate across multiple functions and contribute to the transfer and qualification of analytical methods. This is a hands-on laboratory role that plays a key part in enabling Moderna’s mission to deliver mRNA medicines globally. You’ll also have exposure to Generative AI tools that enhance documentation, testing workflows, and lab efficiency.

Here’s What You’ll Do:

Your key responsibilities will be:

• Executing GMP-compliant QC Molecular Biology methods including Sanger Sequencing, Agarose Gel Electrophoresis, UV/Vis, protein concentration analysis, and qPCR.

• Supporting analytical testing for raw materials, excipients, drug substance, and finished products using techniques such as ELISA and Cell-Based Potency assays.

• Participating in the transfer and qualification of Bioassay methods to and from internal and external labs, in collaboration with AS&T.

• Handling sample management activities including preparation, shipment, and receipt of samples for contract lab testing.

• Maintaining compliance through proper data entry using Good Documentation Practices (GDP).

• Performing environmental monitoring and critical utility sampling activities, as required.

Your responsibilities will also include:

• Supporting the generation of QC data to back other studies and development efforts.

• Conducting routine laboratory operations: reagent preparation, equipment maintenance, and housekeeping.

• Participating in equipment and method qualification efforts.

• Assisting with troubleshooting assay methods and lab equipment to ensure consistency and accuracy.

• Supporting audit readiness and contributing to regulatory and internal audits.

• Writing and revising SOPs, protocols, and reports in alignment with GMP expectations.

• Authoring or participating in quality system documentation including deviations, CAPAs, change controls, and investigations.

• Establishing and maintaining a clean, compliant, and safe laboratory environment.

The key Moderna Mindsets you’ll need to succeed in the role:

• “We digitize everywhere possible using the power of code to maximize our impact on patients.” In this hands-on lab role, you'll embrace digital systems and AI-enabled solutions that enhance lab data management, automate reporting, and improve the efficiency of testing workflows — playing a direct part in scaling our platform with precision.

• “We obsess over learning. We don’t have to be the smartest, we have to learn the fastest.” As Bioassay techniques evolve and new methods are transferred or qualified, you’ll thrive in a learning-driven environment, rapidly mastering new tools, platforms, and procedures that support our GMP compliance and product quality.

Here’s What You’ll Bring to the Table:

• BSc in a relevant scientific discipline with 5 years Quality Control experience in a cGMP organization with a focus in Molecular Biology and DNA Sequencing.

• Hands on experience with molecular biology techniques including, but not limited to, gel electrophoresis, qPCR, Sanger Sequencing and Cell-Based Potency testing.

• Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred.

• Working experience in a GMP environment.

• Ability to collaborate effectively in a dynamic, cross-functional matrix environment.

• Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.

• Proven ability to conduct investigations.

• This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.

• 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.

• Best-in-class healthcare, plus voluntary benefit programs to support your unique needs

• A holistic approach to well-being with access to fitness, mindfulness, and mental health support

• Family building benefits, including fertility, adoption, and surrogacy support

• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown

• Savings and investments to help you plan for the future

• 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 [email protected]. 

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