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
Our team is seeking a motivated and detail-oriented Research Associates with strong hands-on experience in chromatographic analysis to support in-process, release, and stability testing for the MAP program. In this role, you will perform routine cGMP QC testing using HPLC/UPLC methods (reverse-phase, SEC, IEX), Agilent systems, and additional supporting assays. You will also perform HPLC/UPLC method development and troubleshooting to support early-phase clinical QC.
As part of a growing QC department, you will work in a collaborative, fast-paced, and cross-functional environment
What you'll do
Perform routine QC in-process, release, and stability testing using HPLC/UPLC methods including reverse-phase, SEC, and IEX
Perform HPLC/UPLC method development and troubleshooting in collaboration with senior scientists to support the QC workflow
Prepare samples, operate Agilent systems, verify system suitability, and ensure analyses meet method and specification requirements
Execute complementary analytical assays such as UV-Vis, pH, surface tension, and mechanical tests
Maintain complete, accurate documentation in compliance with cGMP, ALCOA+, and data integrity requirements
Conduct routine instrument care (solvent flushes, column care, daily checks)
Process and review chromatographic data in Agilent OpenLab CDS
Support method qualification, validation, and transfer activities by executing protocols and recording observations
Maintain calibration, maintenance, and service records for analytical instrumentation
Write and maintain key technical documentation including SOPs, analytical protocols, technical reports, and audit-ready records; contribute to regulatory submissions
Collaborate cross-functionally with QC, Analytical Development, Process Development, Manufacturing, and Regulatory teams to enable program success
Who you are
Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or related field with 1–3 years of experience; or a master’s degree with relevant laboratory experience
Hands-on experience operating HPLC/UPLC systems; Agilent systems and OpenLab CDS experience strongly preferred
Practical experience with chromatographic techniques including reverse-phase, SEC, and IEX
Experience supporting QC release or stability testing in a GMP-aligned/GLP environment
Strong attention to detail and ability to follow SOPs precisely
Excellent documentation practices and understanding of data integrity
Strong organizational skills with the ability to manage multiple workflows and prioritize effectively in a fast-paced environment
Excellent verbal and written communication skills and comfort working within interdisciplinary teams
Compensation: The anticipated base salary range for this position is $60,000 - $75,000. 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 onsite, 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.
Skills Required
- Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related field with 1–3 years of experience, or a master’s degree with relevant laboratory experience
- Hands-on experience operating HPLC/UPLC systems
- Experience with Agilent systems and OpenLab CDS
- Practical experience with reverse-phase, SEC, and IEX chromatography
- Experience supporting QC release or stability testing in a GMP-aligned or GLP environment
- Strong attention to detail and ability to follow SOPs precisely
- Excellent documentation practices and understanding of data integrity
- Strong organizational skills and ability to manage multiple workflows and priorities
- Excellent verbal and written communication skills and ability to work within interdisciplinary teams
What We Do
Terrestrial Bio, formerly Vaxess Technologies, is a biotech company developing a proprietary temperature-stable microarray patch (MAP) and applicator platform for delivering next-generation therapeutics, initially focusing on GLP-1 treatments. Its needle-free patches are designed for self-administration, eliminate refrigeration and sharps, and provide rapid or sustained delivery. The company is expanding automated manufacturing and preparing its platform for clinical trials and commercialization of next-generation medicines.
