Sr. Manufacturing Automation Engineer – Drive Innovation in Advanced Manufacturing
Listed on 2026-06-21
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Engineering
Manufacturing Engineer, Quality Engineering, Validation Engineer, Process Engineer -
Manufacturing / Production
Manufacturing Engineer, Quality Engineering, Validation Engineer
Sr. Manufacturing Automation Engineer – Drive Innovation in Advanced Manufacturing
Pay Rate: $48–56/hr
Schedule:
Monday–Friday, 8:00am–5:00pm
Assignment Length: 1 year contract
We are hiring an experienced Sr. Manufacturing Automation Engineer to support our client
, a leader in life‑changing health technology, at their Scarborough, ME facility. This is a high‑priority opening offering competitive pay ($48–56/hr) and a full‑time, 1‑year contract with an innovative and highly respected organization.
This is a hands‑on, senior‑level engineering role ideal for someone who enjoys leading automation improvements, solving complex manufacturing problems, and driving quality and efficiency in regulated environments - all while working with cross‑functional teams and cutting‑edge technology.
Typical daily duties:- Support manufacturing processes while driving quality, cost‑savings, and continuous improvement initiatives
- Lead automation equipment upgrades related to safety, obsolescence, and process optimization
- Troubleshoot machine logic, electromechanical systems, and process controls to resolution
- Conduct root cause analysis, FMEA, DOE, validation testing, and data analysis
- Develop and revise SOPs, validation protocols, risk assessments, and manufacturing documentation
- Manage cross‑functional projects and collaborate with the Project Management Office
- Mentor engineers and technicians while supporting training and process expertise
- Ensure compliance with cGMP, FDA, ISO, and other regulatory requirements
- Bachelor’s degree in Engineering (or equivalent experience) with 7+ years in a manufacturing environment
- Strong experience with Lean Six Sigma / DMAIC
, structured problem solving, and change management - Background in FDA, ISO, GMP, cGMP, and ISO 13485 regulated environments
- Technical expertise in automation, fabrication principles, CAD, materials testing, and statistical analysis
- Proficiency with Microsoft tools (Excel, PowerPoint, Power BI) and engineering documentation
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