Moderna · 6 hours ago
Associate I, Quality Control
Norwood, MA
Full-time
Onsite
Entry Level
$54K/yr - $86K/yr
2+ years expModerna is a pioneering company revolutionizing medicine through mRNA technology. As an Associate I in Quality Control, you will ensure the quality of raw materials and mRNA drug products through testing and collaboration with technical teams, contributing to both commercial and clinical programs.
BiotechnologyGeneticsHealth CareMedicalPharmaceuticalTherapeutics
No H1B
U.S. Citizen Only
Responsibilities
Performing in-process and release testing for raw materials, drug substance, and mRNA drug products in compliance with cGMP requirements
Generating critical testing data in support of both commercially approved products and clinical studies
Collaborating with development teams for method transfers and qualification, expanding QC Bioassay lab capabilities including sequencing and qPCR
Supporting the development, implementation, and maintenance of lab operational systems
Leading or contributing to the execution of continuous improvement projects across the QC Bioassay function
Participating in audit preparation and ensuring regulatory compliance for the lab
Investigating and resolving technical issues, assay performance concerns, and equipment-related challenges
Conducting deviation investigations and supporting technical assessments
Assisting in equipment qualification, validation, and maintenance activities
Representing the QC Bioassay team in the absence of management and participating in Tier meetings and resource scheduling
Providing on-the-job training (OJT) and acting as a mentor for junior analysts
Writing and revising SOPs, protocols, and technical reports with adherence to Good Documentation Practices (GDP)
Ensuring data integrity, training compliance, and execution of tasks according to SOPs and internal guidelines
Responding to CTU alarms and contributing to a safe, inclusive, and collaborative laboratory culture
Qualification
Required
Education: BS in a relevant scientific discipline (Biochemistry)
Experience: 2+ years of experience
Demonstrated aptitude or ability to learn: Able gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards and guidance's
This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work
At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship
Preferred
A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative
Benefits
Best-in-class healthcare coverage, 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 investment opportunities to help you plan for the future
Location-specific perks and extras
Company
Moderna
Moderna Therapeutics is a biotechnology company that specializes in vaccines and drug development.
1001-5000 employees
Funding
Current Stage
Public CompanyTotal Funding
$4.56BKey Investors
Coalition for Epidemic Preparedness InnovationsAres ManagementU.S. Department of Health & Human Services
2025-12-18Grant· $54.3M
2025-11-20Post Ipo Debt· $600M
2024-07-02Grant· $176M
Leadership Team
Stephane Bancel
Founding CEO
Kenneth Chien
Co-Founder
Recent News
2026-01-22
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2026-01-22
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