Onsite cGMP Biotech Formulation Technician

Terrestrial; Woburn (MA); On-site; USD 71,635,000 - 85,962,000; Full time

Job summary

Terrestrial Bio, Inc. in Woburn (moving to Allston in November 2026) is seeking a hands-on operator to join our cGMP manufacturing team. You will run formulation equipment, perform in-process testing, and complete batch records to help turn our Tacterra MAP platform into product.

The ideal candidate has 2+ years in a regulated environment, strong lab technique, solid documentation, and the ability to work independently and with a team in a clean room setting.

Qualifications

• 2+ years in a regulated environment (chemical, biotech, medical device, or biopharmaceutical).
• High school diploma required; associate’s degree or trade certification preferred.
• Strong lab technique — pipetting, weighing, mixing solutions, aliquoting, documentation.
• Comfortable working in both laboratory 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

Lab technique

Documentation

Pipetting

Independent worker

Education

High school diploma

Associate degree or trade cert

Tools

Fluid dispensers

Mixers

Pumps

Filtration systems

Job description

Terrestrial Bio, Inc. in Woburn (moving to Allston in November 2026) is seeking a hands-on operator to join our cGMP manufacturing team. You will run formulation equipment, perform in-process testing, and complete batch records to help turn our Tacterra MAP platform into product.

The ideal candidate has 2+ years in a regulated environment, strong lab technique, solid documentation, and the ability to work independently and with a team in a clean room setting.