Engineer I/II, Process Development
About the role
Terrestrial Bio, Inc. 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.
Responsibilities
- Leverage your creativity, hands-on technical skills, and process engineering fundamentals to: Characterize and improve manufacturing process unit operations by designing, executing, and analyzing process development experiments; communicate results via written reports and oral presentations to internal and project teams
- Support manufacturing scale-up through hands-on assessment of novel equipment, workflows, analytical techniques/PAT, and process configurations
- Support phase-appropriate cGMP manufacturing operations by drafting, revising, and reviewing process development histories, master batch records, process and equipment O&M SOPs, and other manufacturing documentation within Terrestrial’s Quality Management System
- Develop and implement new or improved processes and controls to increase quality and throughput
- Design tools, fixtures, and machines for manufacturing Terrestrial’s products
- Collaborate closely with cross-functional teams to support product development and manufacturing activities
Requirements
- B.S. in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or a related discipline with 0-2 years of experience (internship, co-op, or academic research experience) for Process Engineer I and 3+ years of relevant hands-on experience in medical devices or pharmaceutical development/manufacturing for Process Engineer II
- Experience with automated manufacturing equipment or process development strongly preferred
- Hands-on experience designing, executing, and analyzing process development experiments, with strong data analysis and communication skills
- Familiarity or experience working in a cleanroom and/or a biomedical laboratory environment
- Comfort standing or sitting for up to 8 hours, and performing tasks on laboratory benchtops and within glovebox isolators
- Relevant direct experience in medical devices or pharmaceuticals — internship, co-op, or prior work experience all count
- Excellent time and project management skills, with a proven ability to meet goals and deadlines
- Demonstrated ability to learn new skills and fields quickly, think independently, and collaborate across diverse, multidisciplinary teams
Qualifications
- Willingness to be onsite 5 days per week until relocation to a new, custom facility in Allston MA planned for Q4 of 2026
- Location: Woburn, MA
Skills
- Technical expertise in manufacturing process unit operations
- Data analysis and communication skills
- Collaborative problem-solving abilities
- Experience with automated manufacturing equipment
Benefits
- Competitive compensation range: $60,000 - $90,000
- Onsite expectations: Majority of roles are either onsite or hybrid
- Dynamic work environment
- Equal opportunity employer
Pay
The anticipated base salary range for the Engineer I - Engineer II position is $60,000 - $90,000. Actual compensation will be determined based on a variety of factors including experience, qualifications, and internal equity.
Schedule
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 5 days per week.