Senior Manufacturing Engineer
Listed on 2026-08-08
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Engineering
Quality Engineering, Manufacturing Engineer, Validation Engineer, Systems 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.
Woburn & Allston, Massachusetts
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 At Terrestrial Bio, Manufacturing Engineering is not a support function. It is the technical foundation that transforms innovative product concepts into robust, compliant, and scalable manufacturing operations.
The decisions made today will determine our ability to successfully transition from clinical manufacturing to commercial production while maintaining product quality, regulatory compliance, and operational excellence. We are building our manufacturing organization from the ground up. We need a highly experienced engineer who can independently lead complex technical initiatives, establish engineering best practices, and serve as a technical authority across manufacturing, validation, automation, and quality.
The Senior Manufacturing Engineer III is a senior technical leader responsible for implementing and optimizing the manufacturing systems that will support Terrestrial Bio’s next phase of growth. This role will lead equipment integration, process validation, technology transfer, and continuous improvement initiatives while helping establish the engineering standards, documentation, and manufacturing processes that will support a highly automated manufacturing operation. This is not simply a production support role.
It is a build role with significant technical ownership. The successful candidate will help design the manufacturing systems, engineering processes, and operational infrastructure that enable Terrestrial Bio to scale efficiently while maintaining compliance, product quality, and operational agility.
- Lead technical implementation and integration of highly automated equipment and processes, including commissioning, qualification (IQ/OQ/PQ), technology transfer, and site expansion/startup activities.
- Develop manufacturing engineering standards, SOPs, equipment lifecycle documentation, and validation documentation to support a robust, compliant, and scalable operation.
- Establish cross-functional partnerships with Automation, Quality, Facilities, Process Development, and Manufacturing Operations; lead investigations, change controls, CAPAs, root cause analyses, and continuous improvement initiatives to improve reliability, yield, throughput, and OEE.
- Serve as a senior technical resource and mentor, collaborate with suppliers on FAT/SAT and startup, and support regulatory activities.
The Senior Manufacturing Engineer III is responsible for providing technical leadership and execution for manufacturing engineering activities supporting Phase 3 commercial manufacturing of a highly automated pharmaceutical-medical device combination product manufactured in ISO Class 5 isolator environments and reports to the Senior Director of Manufacturing Engineering.
What Makes Someone a Strong Fit- Experience with transfer, installation, startup, and integration of highly automated manufacturing systems, including custom automation and OEM equipment.
- Experience operating within Grade A/ISO Class 5 or aseptic/low bioburden manufacturing environments.
- Develop and execute qualification protocols including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for manufacturing equipment, facilities, utilities, and ancillary systems.
- Develop, review, and revise manufacturing engineering documentation including protocols, reports, work instructions, standard operating procedures (SOPs), engineering specifications, and equipment lifecycle documentation.
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