Scientist I, Bioassay

Posted Yesterday
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Woburn, MA, USA
In-Office
109K-123K Annually
Mid level
Healthtech • Biotech • Pharmaceutical
The Role
Develop and optimize cell-based functional bioassays for preclinical research and GMP lot release testing involving proteins, antibodies, peptides, and RNA. Execute compliant testing, analyze data statistically, maintain laboratory records, prepare reports for regulatory filings, and contribute to study design and translational research supporting IND submissions.
Summary Generated by Built In

Scientist I, Bioassay

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 a talented, collaborative, and highly motivated individual to join our core team of preclinical scientists and engineers contributing to the advancement of novel drug delivery modalities. This role is designed for a versatile researcher. You will play a key role in bioassay development to support preclinical research and GMP lot release testing, including the execution of functional assays to ensure biological performance of drug product. This is a unique opportunity to be part of an emerging company bringing innovative microneedle therapeutic delivery technology to the global market.

What you'll do

  • Develop and optimize cell-based functional assays to support preclinical research and GMP lot release testing for targets that may include proteins, antibodies, peptides, and RNA

  • Execute routine functional testing to ensure biological integrity of drug product following GLP/GMP standards as needed, adhering to good documentation practices and ensuring compliant lab operations and workflows

  • Analyze the data using suitable statistical methods and deliver interpretation for communication of results to the team

  • Maintain accurate laboratory records, generate data summaries and compile reports to support regulatory filings

  • Contribute collaboratively to study design, protocols, and report writing; independently navigate your own schedule to complete priority tasks and communicate findings to the team.

How you'll impact

  • Contribute to translational studies that directly advance IND (Investigational New Drug) filings

  • Challenging, technically fulfilling role at the intersection of engineering and biological efficacy

  • This position offers tangible career growth opportunities

Who you are

  • Recent PhD with post doc in a relevant area or Master’s degree with 4+ years relevant industry experience

  • Significant experience with aseptic mammalian cell culture is required

  • Solid understanding of experimental controls and data interpretation is required

  • PhD or Master degree in Molecular and Cell Biology, Biochemistry, or a related life sciences field

  • Experience with functional assays (e.g. ELISA) and analytical methods (e.g, protein quantification) is highly preferred

  • Experience with animal models is preferred, ideally rat or pig models

  • Strong organizational skills, attention to detail, and initiative appropriate for a fast-paced environment

  • Strong verbal and communication skills with a commitment to working collaboratively within an interdisciplinary team

Compensation: The anticipated base salary range for this position is $109,000 – $123,000. 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 until relocation to a 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

  • Recent PhD with postdoctoral experience in a relevant field, or a master's degree with 4+ years of relevant industry experience
  • Degree in Molecular and Cell Biology, Biochemistry, or a related life sciences field
  • Significant experience with aseptic mammalian cell culture
  • Strong understanding of experimental controls and data interpretation
  • Experience with functional assays such as ELISA and analytical methods such as protein quantification
  • Experience with animal models
  • Strong organizational skills, attention to detail, and initiative
  • Strong verbal and written communication skills and ability to collaborate within an interdisciplinary team
  • Willingness to work onsite 4-5 days per week in Woburn or Allston, Massachusetts
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The Company
71 Employees
Year Founded: 2011

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.

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