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# Engineer Ii/Iii , Formulation

- **Company:** Vaxess Technologies
- **Location:** Woburn, MA, United States
- **Experience:** Experienced
- **Salary:** $72,000 - $91,000
- **Contract:** Permanent contract
- **Skills:** Service Pack, GXP
- **Published:** November 8, 2026
- **Apply:** https://www.careerbuilder.com/job-details/engineer-ii-iii-formulation-woburn-ma--e3c7cf17-4b74-40a2-acce-e39ee37234ec

## About the Role

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.

## 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