Specialist, Quality Assurance On-the-Floor (Drug Substance)

at  Moderna

HERE’S WHAT YOU’LL BRING TO THE TABLE:

Bachelor’s Degree in a science field (e.g., Biology, Microbiology, Chemistry, Pharmacy, Engineering) or equivalent combination of education and experience
3 – 5 years of pharmaceutical or related work experience with emphasis on current Good Manufacturing Practices
Sterile drug product manufacturing experienced preferred
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.
We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:
Quality healthcare and insurance benefits
Lifestyle Spending Accounts to create your own pathway to well-being
Free premium access to fitness, nutrition, and mindfulness classes
Family planning and adoption benefits
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
Educational resources
Savings and investments
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.
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 proud to be an equal opportunity workplace and is an affirmative action employer.
Moderna is committed to equal employment opportunity 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. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com . (EEO/AAP Employer)

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.
Moderna is seeking a dedicated Quality Assurance Specialist for our Melbourne facility to ensure the highest quality standards in the production of mRNA drug substances. In this vital role, you will be on the manufacturing floor, providing real-time quality oversight and making pivotal decisions to maintain compliance with cGMP standards. You’ll collaborate with a cohesive team and cross-functional departments, balancing technical success with strict adherence to quality systems. Your role is crucial in supporting Moderna’s mission to strengthen pandemic resilience through groundbreaking mRNA technology.

HERE’S WHAT YOU’LL DO:

Within 3 Months, You Will…
Familiarize yourself with Moderna’s manufacturing processes and quality systems.
Begin providing on-the-floor quality support, ensuring compliance with GMP standards.
Start conducting routine walkthroughs and monitoring operations to ensure adherence to SOPs and manufacturing documentation.
Within 6 Months, You Will…
Enhance your decision-making skills, effectively managing and escalating quality issues impacting operations.
Collaborate with manufacturing and support teams on deviations and reviews.
Contribute to authoring and reviewing SOPs and Work Instructions, ensuring regulatory compliance.
Within 12 Months, You Will…
Establish yourself as a key player in enforcing GMP compliance and operational efficiency on the production floor.
Demonstrate significant improvements in operational efficiency and risk mitigation.
Be recognized for your ability to independently handle quality decisions and ensure the highest standards in our manufacturing processes.