Sr. Manufacturing Automation Engineer – Drive Innovation in Advanced Manufacturing
Listed on 2026-06-19
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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.
TypicalDaily 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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