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Terrestrialbio

Technician, Formulation

Woburn, MAOnsite · United States
FullTime · Product Development
POSTED 31 JUL
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Role
101 days opentrue age
Posted 31 Jul
Payats field
$25–30 / hourposted
▼ −36% vs market median $90k
$52k$154k
Market p25–p75
$55k–$154k
United States · n=21890 · 365d to 6 Nov
CompanyTerrestrialbio →
11open roles
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Closed · 30d
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416,798open · Other
Opened · 7d
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All tracked boards · live 10 Nov · n=416,798

Location: Woburn, Moving to Allston in November 2026 · Onsite

About Terrestrial Bio, Inc.

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.

Why this role

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.

What you'll do

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

Who you are

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

Compensation: 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.

Onsite expectations: 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.

Location: 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.

Source · TerrestrialbioFirst seen 7 NovOriginal ↗