Analyst, Quality Control, Chemistry & Stability

The Role:

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

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

Modernas 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 Australias 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 Australias 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. Were inviting visionary professionals to be part of this transformative journey making a tangible impact on global health security.

In this lab-based position reporting to the Associate Director of Quality Control you will play a key role in performing cGMP QC testing to support Chemistry Release and Stability functions. As a QC Analyst you will also support global GMP stability programs through a variety of operational and technical activities including sample set downs pulls shipments data trending and statistical analysis. You will work in full compliance with cGMP standards FDA EU and ICH regulations while contributing to method transfers and ongoing method qualification projects. This role is hands-on detail-driven and situated at the intersection of operational execution and scientific rigorideal for someone ready to help scale and shape our QC capabilities. This is an individual contributor position based at our Melbourne Resilience site.

Heres What Youll Do:

Your key responsibilities will be:

• Perform GMP QC Chemistry methods including HPLC UPLC UV and Particle Analysis via Dynamic Light Scattering

• Execute HPLC (AEX) and NaOH plate reader-based assays to support process stat testing

• Support method transfer projects internally and externally in collaboration with Analytical Sciences & Technology (AS&T) teams

• Execute general lab operational tasks aligned with cGMP including reagent preparation equipment maintenance and good documentation practices

• Provide audit support for both internal and regulatory inspections

• Create review and revise SOPs protocols and reports aligned with evolving quality standards and compliance frameworks

Your responsibilities will also include:

• Support all stability program operations: perform sample set downs pulls inventory checks labeling and data entry in LIMS and inventory systems

• Maintain and trend stability data using statistical analysis; produce stability tables charts protocols and final reports

• Troubleshoot assay methods and lab equipment as needed

• Author or contribute to quality system documentation such as investigations deviations CAPAs and change controls

• Assist in the continued optimization of stability and QC workflows ensuring seamless compliance and operational readiness

The key Moderna Mindsets youll need to succeed in the role:

• We obsess over learning. We dont have to be the smartestwe have to learn the fastest.
  In a technically evolving environment like Modernas your success in this QC role hinges on your ability to rapidly absorb new testing technologies regulatory standards and evolving data workflows. Your mindset must be tuned to constant growth and curiosity.

• We digitize everywhere possible using the power of code to maximize our impact on patients.
  This role engages heavily with digital platforms like LIMS for sample tracking inventory control and data analysis. Embracing digital workflows and analytical tools is key to ensuring speed precision and scalability in QC operations.

Heres What Youll Bring to the Table:

• BSc in a relevant scientific discipline (Chemistry preferred) with 5 years Quality Control experience in a cGMP organization with a focus in Analytical Chemistry

• Hands on experience with analytical chemistry techniques including but not limited to HPLC UPLC particle analysis and plate reader-based assays.

• 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 Modernas site full-time. This position is not eligible for remote work.

• As part of Modernas 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. Thats why our global benefits and well-being resources are designed to support youat 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

• Savingsandinvestments 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 theinfrastructure 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 peopleare the driving force behind our scientific progress and our 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 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 persons 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.

Were 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 .

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