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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.
Terrestrial is transforming the delivery of next-generation therapies, starting with GLP-1.
Terrestrial's proprietary Tacterra™ microarray patch (MAP) and applicator platform consists of a patch resembling an adhesive bandage, which is applied with a preloaded applicator and removed after a few minutes. Once applied, each patch delivers bioactive tips into the skin, which dissolve quickly into the body, rapidly releasing their therapeutic payload. Designed for self-administration, the temperature-stable Tacterra™ platform enables precise, controlled delivery of a wide range of therapeutics without medical sharps or refrigeration.
Terrestrial has generated strong clinical and in‑vivo proof of concept across multiple molecules. For more information, visit www.terrestrialbio.com.
This is a direct, hands‑on seat in cGMP manufacturing — you’ll be the one operating the equipment and executing the batch records that turn our platform into product. You’ll work with real formulation equipment (fluid dispensers, mixers, pumps, filtration systems), run the in‑process testing that keeps production on spec, and see your work move straight into the pipeline. It’s a strong entry point into regulated biotech manufacturing, with room to grow as the operation scales.
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
2+ years of relevant experience in a regulated environment (chemical, biotech, medical device, or biopharmaceutical); clean room experience preferred
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
Strong written and verbal communication, attention to detail, and the ability to work independently and on a team
An entrepreneurial drive to make an impact on global human health
The anticipated compensation range for this position is $25 - $30 per hour. Actual compensation will be determined based on a variety of factors including experience, qualifications, and internal equity.
The majority of our roles at Terrestrial are either onsite or hybrid, which allows us to meet both business and team needs. Candidates applying must be willing to be onsite 4-5 days per week.
Woburn, MA and our new, custom facility in Allston MA planned for Q4 of 2026.
At Terrestrial, we're bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. We aim to recruit, employ, train, compensate and promote regardless of race, religion, color, national origin, sex, gender identity or expression, sexual orientation, disability, age, or veteran status.