Associate II, Quality Control

{ "jobLocation" : { "@type" : "Place", "address" : { "@type" : "PostalAddress", "addressCountry" : "United States of America", "addressLocality" : "USA-MA-Marlborough-293 Boston Post Road" } }, "hiringOrganization" : { "name" : "ModernaTX, Inc.", "@type" : "Organization", "sameAs" : "" }, "identifier" : { "name" : "Associate II, Quality Control", "@type" : "PropertyValue", "value" : "R19492" }, "datePosted" : "2026-07-21", "employmentType" : "FULL_TIME", "title" : "Associate II, Quality Control", "description" : "The Role Moderna is seeking a Candidate based at their Marlborough, MA site. The Individual will support cGMP microbiology methods for QC raw material, plasmid, drug substance, Stability, finished product testing for mRNA products produced and Environmental and critical utilities monitoring at Moderna’s manufacturing facility. This individual will contribute to non-testing projects and activities as needed example document certification, monthly biosafety cabinet cleaning etc. This position will be working a 10-h Shift. Here's What You’ll Do Execute compendial microbiological testing, and other methodologies as needed. Perform methods such as Endotoxin, Bioburden, Environmental Monitoring, Microbial identification, Culture Purity, Support testing for in-process samples, drug substance and drug product, including generation of testing data to support clinical studies. Assist in development, implementation, and maintenance of general laboratory operational systems in accordance with cGMP requirements. Perform general laboratory support activities including reagent preparation, equipment maintenance, weekly and monthly cleaning of the BSCs, Document Certification etc. Stock and perform inventory of lab supplies. Establish and maintain a safe laboratory working environment. Here’s What You’ll Need (Basic Qualifications) BS in a relevant scientific discipline with a minimum of 0 - 2 years (or MS in a relevant scientific discipline with 1 year) Quality Control experience in a cGMP organization Excellent troubleshooting and ability to communicate issues in a scientifically sound and understandable way. Familiarity with electronic databases (e.g. LIMS, SAP, LMS, or equivalent software) Strong written and oral communication skills as well as organizational skills Ability to prioritize, manage and complete multiple projects and tasks in a fast-paced environment efficiently and independently. Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between. Competitive 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 planning benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, 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 salary range for this role is $63,200.00 - $100,900.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the