Find Jobs
Find Jobs Near You – Available Work in Your Location
Looking for Process Engineer
Career Insights for Process Quality Engineer
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Connecticut data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Process Quality Engineer evaluates production processes and performance in manufacturing. Develops engineering to improve the quality of existing production processes or develops new processes to improve quality and efficiency.
$91,713 / year median in Connecticut
-3% projected decline
Job Description
We're looking for a Process Engineer to own and improve our injection molding and secondary manufacturing processes in a regulated medical device environment. You'll make sure our processes are reliable, compliant, and produce consistent quality — and you'll be the go-to technical expert for the production floor. What you'll do Own the manufacturing processes for your assigned lines — set the critical parameters, keep them in control, and troubleshoot when things drift. Use SPC and capability data (Cp/Cpk) to catch problems early and drive them out. Run process validations (IQ/OQ/PQ) and keep documentation current — process flows, pFMEAs, control plans, work instructions, validation reports. Work with Quality on nonconformances, deviations, CAPAs, and complaints, and represent manufacturing in audits. Support new product launches — join design reviews, flag manufacturability issues early, and build out the validation plan. Lead continuous improvement work (scrap, yield, cycle time, downtime) using Lean/Six Sigma tools like DMAIC and 8D. Train operators and techs, and mentor junior engineers. Requirements Bachelor's in Mechanical, Plastics, Manufacturing, or Industrial Engineering (or similar). 3-7 years in manufacturing/process engineering. Injection molding experience in a regulated environment — medical device experience is a strong plus. Solid grounding in SPC, process validation, pFMEAs, control plans, and root-cause problem solving. Familiarity with ISO 13485 and FDA QSR preferred; scientific molding knowledge a plus. Comfortable spending real time on the shop floor, juggling multiple priorities. To be considered, please apply with a resume. If you have any other questions you can reach out to Shane Burch at (904) 420-6296 or shane.burch@gogpac.com