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Moderna · 17 hours ago

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

Norwood, MA

Full-time

Onsite

Entry, Mid Level

$74K/yr - $118K/yr

1+ years exp

Moderna is a pioneering company revolutionizing medicine through mRNA technology. The Engineer II role focuses on supporting product labeling, packaging, and storage processes to ensure high-quality mRNA medicines reach patients.

BiotechnologyGeneticsHealth CareMedicalPharmaceuticalTherapeutics

Comp. & Benefits

No H1B

U.S. Citizen Only

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

Qualification

GMP regulationsDrug formulationLabelPackagingTroubleshooting automated systemsSOP writingContinuous improvementCommunication skills

Required

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

Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship