About this role
Senior Process Engineer
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.
The Role
As a Senior Process Engineer at Terrestrial, you will join a team focused on developing innovative manufacturing
processes for production of high-quality therapeutic micro-array patches. Your contributions will support
advancement of pipeline programs through clinical development, as well as establishment of a platform to enable
high-throughput commercial scale manufacturing.
Responsibilities
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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 by assessing novel equipment, workflows, analytical techniques/PAT, and
process configurations
Support manufacturing operations by incorporating equipment and process improvements within
established processes and equipment trains, and by revising manufacturing batch records, SOPs, and other
controlled documents to reflect changes; contribute to implementing and maintaining Terrestrial’ Quality
System.
Supervise and mentor junior engineer(s) and technicians, including a direct report
Collaborate closely with cross-functional teams to support product development and manufacturing
activities
Qualifications
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BS or higher in Engineering (Mechanical, Biomedical, Manufacturing, Materials, or related)
7 – 9 years of relevant, hands-on R&D experience within the medical device or biopharmaceutical
industries; experience working on combination products in a GMP environment is highly desirable
Demonstrated success using empirical and first-principles models to inform and analyze experiments;
experience with statistical methodologies and working with large data sets (e.g. Six Sigma, DoEs,
multivariate techniques) is a plus
Excellent time and project management skills and proven ability to meet goals and deadlines
Demonstrated abilities to learn new skills and fields, creatively solve challenging technical problems, think
independently, and work collaboratively in diverse multidisciplinary teams
Entrepreneurial spirit and drive to positively impact global human health
The anticipated base salary range for this position is $107,000 - $130,000. Actual compensation will be
determined based on a variety of factors including experience, qualifications, and internal equity.
Terrestrial Bio, Inc, 11 Cummings Park Drive, Woburn, MA 01801 www.terrestrialbio.com
At Terrestrial, we’re bringing together exceptional talent to drive our product development forward. We value
collaboration, curiosity, and a dynamic work environment. To apply, please submit your CV/resume to
careers@terrestrialbio.com .
Terrestrial Bio, Inc, 11 Cummings Park Drive, Woburn, MA 01801 www.terrestrialbio.com