Moderna · 10 hours ago
Scientist, Analytical Development
Norwood, MA
Full-time
Onsite
Mid, Senior Level
$109K/yr - $175K/yr
3+ years expModerna is a biotechnology company focused on mRNA technology, and they are seeking a Scientist/Manager for their Norwood Technology Center. The role involves leading the Reference Standard strategy and lifecycle management for mRNA programs, collaborating with various teams, and ensuring compliance and traceability in analytical activities.
BiotechnologyGeneticsHealth CareMedicalPharmaceuticalTherapeutics
No H1B
U.S. Citizen Only
Responsibilities
Lead the end-to-end Analytical Reference Standard strategy for RNA, lipid nanoparticle and drug product for mRNA programs in clinical development
Work closely with colleagues within Analytical Development, Process Development, Analytical Tech Operations, Analytical Sciences and Technology and Quality Control teams to manage Reference Standard lifecycle activities (acquisition, qualification, requalification/stability, phase transition change/bridging), and drive timelines using project management tools
Review, track and assess Reference Standard data, and document and communicate findings
Oversee all logistic for Reference Standard, such as aliquoting, storage, inventory, distribution, shipping, and disposal activities to ensure full compliance ad traceability
Demonstrate independent scientific judgment to study design, data interpretation, technical protocols and reports, regulatory filings, and responses to agency queries; Clearly present findings to multidisciplinary teams
Maintain a safe laboratory work environment and be accountable for good documentation practices
Qualification
Required
B.S. with 5-10 years or MS with 3-5 years of relevant industry experience in analytical development, or quality control, or closely related field
Proven ability to manage projects of significant scope and complexity, while meeting all deliverables and timelines
Hand-on experience in data analysis and statistical evaluation
Hand-on experience in analytical method development and analytical reference standard
Experience in documentation and authoring regulatory submission documents in pharmaceutical or biotech industries
Exceptional organizational, communication, and critical thinking skills, and the ability to thrive in an interdependent and idea-rich environment
Excellent interpersonal and collaborative skills
Ability to navigate through ambiguity and rapid growth and adapt to change
This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work
Preferred
GMP analytical-chemistry experience is preferred
Previous hands-on industry experience with analytical development for nanoparticles, RNA, therapeutics, or biologics is a plus and preferred
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
Morningstar.com
2026-01-09
Company data provided by crunchbase