About this role
Senior / Principal Scientist Analytical Method Development Lead
Terrestrial Bio
Location: Allston, MA and Woburn, MA
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
We are seeking an Analytical Method Development (AMD) Lead to drive the analytical method development,
qualification, and validation strategy for the microneedle array patch (MAP) program. This individual will lead the
development of release and characterization methods including HPLC/UPLC, LC-MS, and functional assays and own
the analytical method lifecycle from Phase 2 through Phase 3 IND and commercialization.
This is a senior technical leadership role for a scientist with deep peptide/biologic analytical expertise and a track
record of building robust, regulatory-compliant methods.
What you'll do
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Lead analytical method development for release and characterization assays including RP-HPLC/UPLC
purity, content, SEC, and impurity characterization by LC-MS.
Define and execute the analytical method validation strategy per ICH Q2(R2) and Q14.
Develop the Validation Master Plan (VMP) governing method qualification, validation, transfer, and
lifecycle management.
Establish the impurity characterization strategy for GLP-1 peptide, including oxidation, deamidation, and
related substances.
Lead method transfers to QC and to/from external CROs.
Define the analytical control strategy and specifications for Phase 2 Tox and Phase 3 clinical lots.
Support characterization of reference standards and establishment of bridging strategies.
Author analytical sections of regulatory submissions (IND, CMC) and serve as analytical SME during
inspections.
Guide the development of the potency/functional assay strategy in collaboration with pre-clinical and
formulation teams.
Mentor and develop method development scientists; provide technical leadership across the AMD
function.
Who you are
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Ph.D. in Analytical Chemistry, Biochemistry, or related field with 6+ years relevant experience, OR M.S. with
8+ years in pharmaceutical/biotech analytical method development.
Deep expertise in HPLC/UPLC method development for peptides or biologics.
Hands-on experience with LC-MS for impurity characterization and structural analysis.
Demonstrated experience leading method validation under ICH Q2(R2)/Q14.
Experience developing analytical control strategies and specifications for clinical-stage products.
Strong knowledge of ICH Q6A, Q3A/B/C/D, and FDA/EMA CMC expectations.
Preferred Qualifications
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Experience with GLP-1 peptides or semaglutide analytical methods.
Experience with microneedle/transdermal or drug-device combination products.
Prior experience defining potency or cell-based functional assay strategies.
Experience supporting IND/BLA filings and regulatory interactions.
Experience building and scaling an analytical method development function.
Key Competencies
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Deep technical expertise combined with strategic program thinking.
Strong leadership and mentoring capability.
Excellent scientific writing and regulatory communication.
Ability to balance scientific rigor with program timelines in a fast-paced environment.
Compensation: The anticipated base salary range for this position is $125,000 - $180,000. 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 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.