Engineer II, Drug Product, Manufacturing Science and Technology (MSAT), Label and Pack, Final Storage

Moderna • Norwood, MA

2d • $74,000 - $118,400

About The Position

The Role Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide. This role offers the opportunity to work at the core of Moderna’s GMP operations, supporting product labeling, packaging, and storage processes that ensure our mRNA medicines reach patients with the highest standards of quality. As Engineer II, you will assist in process execution, contribute to troubleshooting, and support continuous improvement initiatives within the label and pack space. Working closely with experienced team members, you'll gain hands-on exposure to operational excellence, compliance, and innovation. You'll play a key role in documentation and investigations, acting as a critical link between Operations and Quality. This is a dynamic position in which you will help shape and strengthen Moderna’s packaging capabilities at the Norwood site.

Requirements

• Bachelor's or Master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, or related field.
• A minimum of 1-3 years of experience in the biotech or pharmaceutical industry, with a focus on drug formulation, filling processes and label and packaging.
• Strong understanding of GMP regulations and guidelines.
• Proven ability to troubleshoot issues related automated systems.
• Strong written and verbal communication skills.

Responsibilities

• Supporting day-to-day technical activities related to both automated and manual label and packaging equipment, as well as the storage conditions of finished drug product.
• Participating in execution and monitoring of packaging and storage processes to ensure optimal performance.
• Drafting and contributing to SOPs related to labeling and packaging workflows, ensuring they meet evolving GMP and regulatory expectations.
• Supporting deviation investigations and implementing corrective and preventive actions (CAPAs).
• Assisting with updates to batch records and controlled documentation within the GMP framework.
• Participating in internal and external audit activities as a subject matter expert in label and packaging.
• Collaborating directly with Process Experts and Technicians to ensure consistent process performance.
• Acting as a liaison between Operations and the Quality organization to enable compliant, high-quality product handling.
• Engaging in continuous improvement initiatives under the guidance of senior team members.
• Ensuring strict adherence to Moderna’s GMP standards while supporting operational readiness and scalability.

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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 1,001-5,000 employees