BioSpace
Overview
2026 Co-Op, Supply Chain, Logistics Engineering — BioSpace. This is a co‑op opportunity in Norwood, MA from January 20, 2026 – June 26, 2025. Applicants must be available for the entire duration of the co‑op. Start date will be January 20, 2026. The Global Supply Chain Organization is seeking top talent to support our mission of delivering mRNA medicines to patients worldwide. As a Summer Co‑Op in Logistics Engineering, you will be part of a high‑performing team dedicated to the development, monitoring, governance, and continuous improvement of cold chain requirements across Moderna’s global network. This internship offers a unique opportunity to gain hands‑on experience in project management, vendor coordination, and process improvement initiatives. You will apply your educational background and develop new technical skills to support pre‑clinical, clinical, and commercial programs—ensuring compliance with industry best practices, regulatory guidance, and internal quality standards. Responsibilities
Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance. Execute tasks as defined in internal guiding documents, including SOPs and work instructions. Apply Good Documentation Practices (GDP) and Data Integrity requirements to maintain accurate and compliant records for audits and inspections. Complete assigned training in line with required learning plans and requalification cadences. Analyze logistics systems and design improvements to enhance efficiency, reduce costs, and improve supply chain performance. Identify process bottlenecks and propose practical, sustainable solutions. Collect and analyze logistics and transportation data to support ongoing projects. Participate in logistics projects from initiation through implementation, including collaborations with 3PLs and carriers. Evaluate and recommend technology and digital solutions (automation, analytics, temperature monitoring tools) to strengthen supply chain operations. Ensure logistics solutions and innovations comply with relevant safety and regulatory standards. Prepare reports and presentations highlighting findings, recommendations, and impacts of implemented solutions related to Quality Management Systems and cold chain requirements. Support shipping validation activities, including Operational and Performance Qualification (OQ/PQ) for active and passive shippers. Assist in developing training materials and supporting knowledge transfer for new shipper solutions or process rollouts. Basic Qualifications
Current student enrolled in a Bachelor’s or master's program in Chemical Engineering, Mechanical Engineering, Supply Chain Management, or a related field. Strong foundation in scientific and engineering principles, with preference for knowledge in thermodynamics and heat transfer. Demonstrated ability to learn and apply GxP regulations (GMP, GLP, GCP, GVP, or others as applicable). Strong communication skills, including technical writing and presentation abilities. Analytical mindset with the ability to evaluate data and identify process improvements. Ability to collaborate effectively in cross‑functional and global team settings. This role requires work authorization in the US without the need for future sponsorship. Immigration sponsorship is not available. Site‑based position, not eligible for remote work. Preferred Qualifications
GPA of 3.5 on a 4.0 scale or equivalent. Ability to work independently and as part of high‑performing teams. Excellent written and verbal communication skills. Desire to contribute to a high‑growth, transformational company that values boldness, relentlessness, curiosity, and collaboration. Benefits and Working Model
At Moderna, we offer benefits and well‑being resources designed to support you at work and home. Examples include free premium access to meditation and mindfulness classes, subsidized commuter benefits, generous paid time off (vacation, sick time, holidays), volunteer time, a discretionary year‑end shutdown, and location‑specific perks. Our working model emphasizes in‑person collaboration with a 70/30 in‑office structure to foster innovation, teamwork, and mentorship. Moderna is a smoke‑free, alcohol‑free, and drug‑free work environment. Equal Opportunities and Accommodations
Moderna is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other protected characteristic. Moderna is an E‑Verify employer in the United States. We provide reasonable accommodations to qualified applicants; contact the Accommodations team at leavesandaccommodations@modernatx.com for assistance. Export Control Notice
This position may involve access to technology or data subject to U.S. export control laws, including EAR. Employment is contingent upon the applicant’s ability to access export‑controlled information in accordance with U.S. law. Only U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. Moderna is unable to sponsor non‑U.S. persons to apply for an export control license.
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2026 Co-Op, Supply Chain, Logistics Engineering — BioSpace. This is a co‑op opportunity in Norwood, MA from January 20, 2026 – June 26, 2025. Applicants must be available for the entire duration of the co‑op. Start date will be January 20, 2026. The Global Supply Chain Organization is seeking top talent to support our mission of delivering mRNA medicines to patients worldwide. As a Summer Co‑Op in Logistics Engineering, you will be part of a high‑performing team dedicated to the development, monitoring, governance, and continuous improvement of cold chain requirements across Moderna’s global network. This internship offers a unique opportunity to gain hands‑on experience in project management, vendor coordination, and process improvement initiatives. You will apply your educational background and develop new technical skills to support pre‑clinical, clinical, and commercial programs—ensuring compliance with industry best practices, regulatory guidance, and internal quality standards. Responsibilities
Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance. Execute tasks as defined in internal guiding documents, including SOPs and work instructions. Apply Good Documentation Practices (GDP) and Data Integrity requirements to maintain accurate and compliant records for audits and inspections. Complete assigned training in line with required learning plans and requalification cadences. Analyze logistics systems and design improvements to enhance efficiency, reduce costs, and improve supply chain performance. Identify process bottlenecks and propose practical, sustainable solutions. Collect and analyze logistics and transportation data to support ongoing projects. Participate in logistics projects from initiation through implementation, including collaborations with 3PLs and carriers. Evaluate and recommend technology and digital solutions (automation, analytics, temperature monitoring tools) to strengthen supply chain operations. Ensure logistics solutions and innovations comply with relevant safety and regulatory standards. Prepare reports and presentations highlighting findings, recommendations, and impacts of implemented solutions related to Quality Management Systems and cold chain requirements. Support shipping validation activities, including Operational and Performance Qualification (OQ/PQ) for active and passive shippers. Assist in developing training materials and supporting knowledge transfer for new shipper solutions or process rollouts. Basic Qualifications
Current student enrolled in a Bachelor’s or master's program in Chemical Engineering, Mechanical Engineering, Supply Chain Management, or a related field. Strong foundation in scientific and engineering principles, with preference for knowledge in thermodynamics and heat transfer. Demonstrated ability to learn and apply GxP regulations (GMP, GLP, GCP, GVP, or others as applicable). Strong communication skills, including technical writing and presentation abilities. Analytical mindset with the ability to evaluate data and identify process improvements. Ability to collaborate effectively in cross‑functional and global team settings. This role requires work authorization in the US without the need for future sponsorship. Immigration sponsorship is not available. Site‑based position, not eligible for remote work. Preferred Qualifications
GPA of 3.5 on a 4.0 scale or equivalent. Ability to work independently and as part of high‑performing teams. Excellent written and verbal communication skills. Desire to contribute to a high‑growth, transformational company that values boldness, relentlessness, curiosity, and collaboration. Benefits and Working Model
At Moderna, we offer benefits and well‑being resources designed to support you at work and home. Examples include free premium access to meditation and mindfulness classes, subsidized commuter benefits, generous paid time off (vacation, sick time, holidays), volunteer time, a discretionary year‑end shutdown, and location‑specific perks. Our working model emphasizes in‑person collaboration with a 70/30 in‑office structure to foster innovation, teamwork, and mentorship. Moderna is a smoke‑free, alcohol‑free, and drug‑free work environment. Equal Opportunities and Accommodations
Moderna is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other protected characteristic. Moderna is an E‑Verify employer in the United States. We provide reasonable accommodations to qualified applicants; contact the Accommodations team at leavesandaccommodations@modernatx.com for assistance. Export Control Notice
This position may involve access to technology or data subject to U.S. export control laws, including EAR. Employment is contingent upon the applicant’s ability to access export‑controlled information in accordance with U.S. law. Only U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. Moderna is unable to sponsor non‑U.S. persons to apply for an export control license.
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