Hands-on cGMP Formulation Technician – Biotech

Terrestrial Bio; Walnut Hill (MA); On-site; USD 34,440 - 41,328; Full time

Job summary

Terrestrial Bio, Inc. in Woburn (moving to Allston in November 2026) is seeking a hands-on manufacturing operator for cGMP formulation operations.

You will run reactors, dispensers, mixers, and filtration systems, executing batch records and in-process tests to keep production within spec. You will work closely with process development and quality teams, ensuring proper documentation, safety, and regulatory compliance while contributing to the scale-up of our MAP platform.

Qualifications

• 2+ years of relevant experience in a regulated environment (chemical, biotech, medical device, or biopharmaceutical); clean room experience preferred.
• Strong lab technique—pipetting, weighing, mixing solutions, aliquoting, documentation.
• Comfortable working in both laboratory and clean room environments.
• Strong written and verbal communication, attention to detail, and ability to work independently and on a team.
• Entrepreneurial drive to make an impact on global human health.

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

Regulated environment experience

Lab technique

Pipetting

Documentation

Independent and team work

Education

High school diploma

Associates degree or trade certification

Job description

Terrestrial Bio, Inc. in Woburn (moving to Allston in November 2026) is seeking a hands-on manufacturing operator for cGMP formulation operations.

You will run reactors, dispensers, mixers, and filtration systems, executing batch records and in-process tests to keep production within spec. You will work closely with process development and quality teams, ensuring proper documentation, safety, and regulatory compliance while contributing to the scale-up of our MAP platform.