Engineer Ii/Iii , Formulation
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Role details
Tech stack
Job description
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 do
- 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
Requirements
Refrigeration, Automation, Leadership, Process Development, Campaigns, Software Patches, Manufacturing/Industrial Processes, Manufacturing, Research & Development (R&D), Current Good Manufacturing Practice (cGMP), * 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)
- Engineer III - BS or MS in Biological Sciences, Chemistry, Biomedical Engineering, Chemical Engineering, or related, with 5+ years of relevant experience (title adjusted to 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.
Benefits & conditions
Compensation: The anticipated base salary range for the Engineer II position is $72,000 - $91,000. The compensation for the Engineer III position is $102,000 - $114,000. Actual compensation will be determined based on a variety of factors including experience, qualifications, and internal equity.
About the company
At Terrestrial, we’re bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. We aim to recruit, employ, train, compensate and promote regardless of race, religion, color, national origin, sex, gender identity or expression, sexual orientation, disability, age, or veteran status.
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