Associate I, Quality Control (Microbiology, Environmental Monitoring) In this role, you will perform routine environmental monitoring and critical utilities (water and process gasses) sampling of the GMP manufacturing facility.
The Quality Control Associate I will also support microbiological testing for GMP QC raw materials, excipients, drug substance, and finished product testing for mRNA products produced at Moderna's manufacturing facility.
The Quality Control Associate may perform projects as assigned.
Here's What You'll Do Perform routine environmental monitoring and critical utility sampling activities.
Conduct analysis of water samples to include TOC, Conductivity, Bioburden, and Endotoxin.
Conduct process gasses testing for Total particulates, Viable Air, Hydrocarbons, and Dewpoint.
Perform routine testing in support of manufacturing processes to include bioburden, sterility, endotoxin, culture purity, and cell stock identity.
Prepare and ship contract laboratory testing samples including those intended for microbiological identification.
Perform general laboratory support activities including equipment maintenance and housekeeping.
May participate in equipment and method qualifications, validations, and method transfers.
Perform data entry utilizing good documentation practices.
Support initiation/closure of quality system records such as environmental monitoring excursion notifications and deviations.
Write/revise standard operating procedures.
Additional duties as may be assigned from time to time.
Here's What You'll Need (Basic Qualifications) BS in a relevant scientific discipline or 5 years Quality Control experience in a cGMP organization with a focus in Microbiology.
This position is site-based, requiring you to be at Moderna's site full-time.
This position is not eligible for remote work.
Here's What You'll Bring To The Table (Preferred Qualifications) A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
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.
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.
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