2026 Co-Op, Drug Product Development

ModernaNorwood, MA
6d$20 - $60Onsite

About The Position

This is a Fall co-op opportunity in Norwood, M A from July 13th-December 11th. Applicants must be available for the entire duration of the co-op. The start date will be July 13th, 2026. The Technical Development (Tech Dev) organization at Moderna designs and scales manufacturing processes for mRNA medicines. Co-ops will join high-performing project teams developing new manufacturing platforms to produce mRNA therapeutics and vaccines for clinical trials and commercial licensure. You’ll apply your educational background while gaining hands-on experience in mRNA synthesis, lipid nanoparticle (LNP) assembly, and drug-product formulation; process characterization using small-scale models; and stability studies, including hold studies simulating clinical in-use stability and compatibility assessments. You will deepen your understanding of control strategies to ensure processes consistently deliver medicines of the highest quality. Product Development creates and matures LNP-based formulations and drug-product processes that deliver performance, stability, and manufacturability. The team develops platform- and program-specific formulations, defines fill-finish and handling strategies, and establishes shelf life and cold-chain readiness to enable reliable technology transfer across sites.

Requirements

  • Current student enrolled in a Bachelor’s or Master’s 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 f undamental 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 the 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.

Nice To Haves

  • GPA of 3.5 on a 4.0 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.
  • Use laboratory, technical and communication skills to generate experimental results, perform data analysis, and document in formal reports including conclusions and recommended next steps.
  • Perform process scale-up, support technology transfer, and provide manufacturing support at internal Moderna, and external contract manufacturing sites.
  • Participate in planning, design, execution, analysis of experiments and formal risk assessments to establish critical process parameters, and overall process control strategies.
  • Optimize the impact of formulation and processing conditions on the stability of mRNA drug pr oduc ts and process intermediates.
  • Review and share relevant academic literature and establish new collaborations with internal research and manufacturing groups.
  • Create scaled-down models, and high-throughput experimental setups for unit operations.
  • Characterize mRNA and lipid nanoparticles through collaboration with the analytical team.
  • Design and execute stability studies, including in-use, hold-time, and compatibility studies, to assess drug product robustness under clinically relevant conditions.
  • Prepare technical reports and present findings in cross-functional meetings.
  • Additional duties 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
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