Engineer I/II, Formulation

Terrestrial Bio, Inc.; Woburn (MA); On-site; USD 62,000 - 91,000; Full time

Job summary

Terrestrial Bio, Inc. in Woburn, MA is seeking an Engineer I/II, Formulation to oversee cGMP formulation operations for the microarray patch platform.

You will ensure batch records, SOPs, and regulatory requirements are followed while mentoring junior staff on manufacturing campaigns. Reporting to the Director of Process Development, you will bridge Research, Manufacturing, Quality, and Automation to scale formulations from R&D to production and drive continuous improvement through new

Qualifications

• BS in Chemical Engineering, Biomedical Engineering, Chemistry, or related discipline; Engineer I 0–2 years of experience.
• Engineer II requires BS or MS in Biological Sciences, Chemistry, Biomedical Engineering, Chemical Engineering, or related discipline, with 3+ years of relevant experience.
• Hands-on formulation process development experience.
• Supervisory experience in a GxP environment preferred.
• Strong documentation practices including authoring and reviewing batch records, SOPs, and work instructions.
• Excellent verbal and written communication, time management, and project management skills.

Responsibilities

• Lead cGMP formulation operations for Microarray Patch manufacturing, ensuring adherence to batch records, SOPs, and regulatory requirements
• Provide hands-on guidance to junior staff and technicians during manufacturing campaigns; train, mentor, and evaluate personnel
• Oversee day-to-day manufacturing floor activities — safety, compliance, scheduling, and troubleshooting — alongside Manufacturing and Facilities
• Drive process development and optimization studies for microarray patch formulations, including excipient optimization
• Act as the liaison between Research and Manufacturing to scale formulation processes from R&D to production
• Identify and implement new technologies and assays to support continuous improvement
• Lead root cause analyses and process development investigations
• Author, edit, and review batch records, SOPs, and work instructions
• Communicate progress, issues, and results to key stakeholders

Skills

Formulation development

GxP experience

Documentation practices

Project management

Cross-functional collaboration

Education

BS in Chemical Engineering

BS in Biomedical Engineering

MS in Chemical Engineering

Job description

Engineer I/II, Formulation

Woburn, Moving to Allston, MA · Onsite

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

You’ll own the handoff that makes or breaks a platform like ours: taking formulations from R&D and turning them into repeatable, compliant manufacturing processes. Reporting to the Director of Process Development, you’ll act as the connective tissue between Research, Manufacturing, Quality, and Automation — with real influence over how our microarray patch formulations get built, optimized, and scaled. You’ll also have hands‑on oversight of formulation campaigns and the technicians running them, giving you both technical depth and early leadership experience.

WHAT YOU’LL WORK ON

• Lead cGMP formulation operations for Microarray Patch manufacturing, ensuring adherence to batch records, SOPs, and regulatory requirements
• Provide hands‑on guidance to junior staff and technicians during manufacturing campaigns; train, mentor, and evaluate personnel
• Oversee day‑to‑day manufacturing floor activities — safety, compliance, scheduling, and troubleshooting — alongside Manufacturing and Facilities
• Drive process development and optimization studies for microarray patch formulations, including excipient optimization
• Act as the liaison between Research and Manufacturing to scale formulation processes from R&D to production
• Identify and implement new technologies and assays to support continuous improvement
• Lead root cause analyses and process development investigations
• Author, edit, and review batch records, SOPs, and work instructions
• Communicate progress, issues, and results to key stakeholders

WHAT YOU BRING

• Engineer I - BS in Chemical Engineering, Biomedical Engineering, Chemistry, or a related discipline; 0–2 years of relevant experience (internship, co‑op, or academic research experience welcomed)
• Engineer II - BS or MS in Biological Sciences, Chemistry, Biomedical Engineering, Chemical Engineering, or related discipline, with 3+ years of relevant experience (title adjusted commensurate with qualifications)
• Strong hands‑on formulation process development experience; able to design and execute studies and analyze results independently
• Prior supervisory experience in a GxP environment preferred
• Strong grasp of Good Documentation Practices, including authoring and reviewing batch records, SOPs, and work instructions
• Excellent verbal and written communication, time management, and project management skills
• Ability to learn quickly, solve challenging technical problems creatively, and work well across diverse, multidisciplinary teams
• Strong attention to detail and root‑cause problem‑solving skills.

The salary range for the Engineer I role is $62,000 to $82,000

The salary range for the Engineer II role is $72,000 to $91,000

Terrestrial Bio, Inc. · 11 Cummings Park Drive, Woburn, MA 01801 · www.terrestrialbio.com