Technician, Product Development

Terrestrial Bio•Woburn, MA
•$25 - $30•Onsite

About The Position

Terrestrial Bio, Inc. is hiring a Product Development Technician to perform hands-on cGMP manufacturing and product development for combination products. The role involves operating equipment, executing batch records, working with medical device components and assembly equipment, and conducting in-process testing. The position also offers opportunities to support Research and Development activities, including prototyping, test method development, design control, and experiments supporting the design and development of next-generation combination products. The role is based onsite in Woburn, Massachusetts, until relocation to a custom facility in Allston, Massachusetts, planned for Q4 2026. Candidates must be willing to work onsite five days per week. The anticipated hourly rate is $25.00–$30.00; actual compensation depends on factors including experience, qualifications, and internal equity.

Requirements

  • At least 2 years of relevant experience in a regulated chemical, biotech, medical device, or biopharmaceutical environment.
  • High school diploma.
  • Strong lab technique, including mechanical testing, weighing, visual inspection, dimensional measurement, computer-aided design, 3D printing, and statistical analysis.
  • Comfort working in both laboratory and clean room environments.
  • Strong written and verbal communication skills, attention to detail, and ability to work independently and as part of a team.
  • Willingness to work onsite five days per week.

Nice To Haves

  • Clean room experience.
  • Associate’s degree or trade certification.

Responsibilities

  • Perform cGMP medical device operations according to documented procedures and batch records.
  • Operate device assembly and testing equipment, including custom assembly fixtures, mechanical testers, laser displacement sensors and controllers, and dimensional measurement equipment.
  • Complete batch records, logbooks, and test records in accordance with Good Documentation Practices.
  • Conduct in-process testing, including visual inspection and physical and mechanical testing.
  • Contribute to root cause analyses and product development investigations.
  • Review documentation for completeness and regulatory compliance.
  • Support process and product development, including design control, test method development, in vivo and ex vivo experiments, custom fixture design, and prototyping.
  • Follow safety guidelines for PPE, chemical handling, and emergency procedures.
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