2026 Co-Op, Analytical Development Strategy

ModernaTX • Norwood, MA

1d • $20 - $60 • Onsite

About The Position

This is a Summer / Fall co-op opportunity in Norwood, MA from July 13, 2026 – December 11, 2026. Applicants must be available for the entire duration of the co-op. Start date will be July 13, 2026 The Technical Development (Tech Dev) organization at Moderna leads process development and phase-appropriate analytical method development and technical transfer to support mRNA therapeutics and vaccines from clinical development through commercial licensure. Within Tech Dev, Analytical Development (AD) leads critical quality attribute (CQA) characterization, release and stability strategies, method lifecycle management, and seamless transfer to Quality Control (QC), enabling efficient tech transfer, scale-up, and regulatory filings. The Co-op will join the AD Clinical Stability team and support development and clinical stability studies for RNA, LNP and DP. This role involves collaborating with other analytical teams to support stability study design; authoring protocols and reports; and performing stability data mining, trending, and statistical analyses. The ideal candidate thrives in a fast-paced, highly collaborative, cross-functional environment and is comfortable working across technical and strategy teams. Integrity, curiosity, strong communication skills, a collaborative mindset, and a commitment to high-quality work are essential for success in this role.

Requirements

• Current student enrolled in a Bachelors or Masters program in Chemical Engineering, Biochemical Engineering, Bioengineering, Biomolecular Engineering, Chemistry, Biochemistry, Biomedical Engineering, Biophysics, Biostatistics, Biotechnology, Mathematics, Molecular Biology, Pharmaceutical Science, Statistics, or a related field
• Strong fundamental scientific and engineering skills for the evaluation of experimental data
• Laboratory skills applicable to bioprocess development and analytical methods
• Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.
• This position is site-based, requiring you to be at Moderna’s site full-time.
• This position is not eligible for remote work.

Nice To Haves

• GPA of 3.5 on a 4 scale or equivalent
• Demonstrated ability to work both independently as well as the ability to contribute to high performing teams.
• Excellent written and verbal communication skills.
• A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Responsibilities

• Work with a team of highly skilled experts to come up to speed on technology and techniques.
• Support stability study strategy and study designs based on practical understanding of ICH stability guidelines and program needs
• Author study protocols and study reports
• Work closely with CMC Quantitative Sciences on stability data analysis and perform data trending to support shelf life extension
• Generate high quality stability documentation to support regulatory submissions and internal communications
• Present development and GMP stability data at cross-functional data review meetings
• Additional duties as may be assigned from time to time.

Benefits

• Free premium access to meditation and mindfulness classes
• Subsidized commuter benefits
• Generous paid time off, including vacation, sick time, holidays, volunteer days, and a discretionary year-end shutdown
• Location-specific perks and extras

What This Job Offers

• Job Type: Full-time
• Career Level: Intern