Technician, Formulation

Terrestrial Bio

Walnut Hill (MA)

On-site

USD 34,440 - 41,328

Full time

14 days+

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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

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 Will Own

  • 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

What you bring

  • 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 range

  • $25 - $30 per hour

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