Hands-On cGMP Formulation Technician – Onsite

Terrestrial Bio, Inc.; Woburn (MA); Hybrid; USD 34,000 - 41,000; Full time

Job summary

Terrestrial Bio, Inc. in Woburn, MA (moving to Allston in Nov 2026) is seeking a hands-on manufacturing operator for cGMP formulation operations. You will run fluid dispensers, mixers, pumps, and filtration systems, execute batch records, and perform in-process testing to keep production on spec.

You will review documentation for regulatory compliance, support process development, follow safety guidelines, and contribute to root cause analyses as the operation scales—onsite 4-5 days a week.

Qualifications

• 2+ years of relevant experience in a regulated environment (chemical, biotech, medical device, or biopharmaceutical); clean room experience preferred.
• Strong lab technique including pipetting, weighing, and solution preparation; meticulous documentation.
• Comfortable working in both lab and clean room environments.

Responsibilities

• Perform cGMP formulation operations according to documented procedures and batch records.
• Operate formulation equipment — fluid dispensers, mixers, pumps, filtration systems
• Complete batch records, logbooks, and test records following Good Documentation Practices
• Run in-process testing: pH, density, filter integrity, API concentration
• Contribute to root cause analyses and process development investigations
• Review documentation for completeness and regulatory compliance
• Support process development efforts as needed
• Follow all safety guidelines — PPE, chemical handling, emergency procedures

Skills

Experience in regulated environment

Lab technique

Attention to detail

Communication (written and verbal)

Independent and teamwork

Entrepreneurial drive

Education

High school diploma

Associate’s degree

Trade certification

Tools

Fluid dispensers

Mixers

Pumps

Filtration systems

Job description

Terrestrial Bio, Inc. in Woburn, MA (moving to Allston in Nov 2026) is seeking a hands-on manufacturing operator for cGMP formulation operations. You will run fluid dispensers, mixers, pumps, and filtration systems, execute batch records, and perform in-process testing to keep production on spec.

You will review documentation for regulatory compliance, support process development, follow safety guidelines, and contribute to root cause analyses as the operation scales—onsite 4-5 days a week.