Sr. Manufacturing Associate I, Drug Substance Operations

Scorpion Therapeutics; Norwood (MA); On-site; USD 85,000 - 115,000; Full time

Job summary

Scorpion Therapeutics in Massachusetts is seeking a Senior Manufacturing Associate I to execute GMP manufacturing processes for mRNA and LNP drug substances, supporting both clinical and commercial vaccines. The role focuses on aseptic processing, formulation, filling, dispensing, and rigorous documentation in sterile environments.

You will use systems such as SAP, VEEVA, DeltaV, and LIMS, participate in safety programs, and collaborate with quality, engineering, and validation teams to ensure

Qualifications

• HS Diploma with 8+ years industry experience or STEM degree with 4+ years.
• Strong GMP knowledge and adherence to safety standards.
• Experience with aseptic processing and manufacturing at clinical and commercial scales.

Responsibilities

• Perform aseptic processing, formulation, filling, and dispensing.
• Ensure documentation compliance in sterile environments.
• Train colleagues and troubleshoot manufacturing processes.

Skills

GMP knowledge

Aseptic processing

Documentation compliance

Education

HS Diploma with 8+ years

STEM degree with 4+ years

Tools

SAP

VEEVA

DeltaV

LIMS

Job description

Role

Senior Manufacturing Associate I in mRNA and LNP drug substance operations, responsible for executing GMP manufacturing processes for clinical and commercial vaccines.

Core responsibilities

aseptic processing, formulation, filling, dispensing, and documentation compliance within sterile environments; utilizing manufacturing systems such as SAP, VEEVA, Delta V, and LIMS; and performing training and troubleshooting.

Qualifications

HS Diploma with 8+ years industry experience, or STEM degree with 4+ years, demonstrating strong GMP knowledge.

Requirements

adherence to safety and GMP standards, precise task execution, and understanding of equipment and process controls.

HighValue

GMP manufacturing, aseptic processing of mRNA/LNP (including chromatography, filtration, nano-mixing), clinical and commercial scale, regulated environment, cross-functional collaboration with quality, engineering, and validation teams, and experience with manufacturing support systems.

Work setup

On-site with a 70/30 in-office model; no travel specified.