Sr. Manufacturing Automation Engineer

Experis; Westbrook (ME); On-site; USD 64,781 - 92,264; Full time

Benefits offered by this job

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

Health Savings Account

401(k), Plus Match

Weekly Pay

Job summary

Experis is seeking a Sr. Manufacturing Automation Engineer in Westbrook, ME. The role involves supporting manufacturing processes and leading automation improvements.

The ideal candidate has a Bachelor's degree in engineering, over 7 years of experience, and proficiency in Lean Six Sigma. They will work in a collaborative environment focused on operational excellence and quality initiatives.

Comprehensive benefits package includes medical, dental, vision plans, and 401(k) matching.

Qualifications

• 7+ years of manufacturing engineering experience.
• Experience in ISO, FDA, or similar regulated environments.
• Strong technical skills in equipment specification and automation.

Responsibilities

• Support manufacturing processes with engineering principles.
• Lead automation equipment upgrades and troubleshooting.
• Design experiments and present findings to teams.
• Create and revise technical documents to ensure compliance.
• Manage project teams and mentor junior engineers.

Skills

Lean Six Sigma principles

DMAIC

Statistical analysis software

Microsoft Office Suite

CAD tools

Education

Bachelor’s degree in engineering or a related field

Job description

Our client, a leader in the healthcare manufacturing sector, is seeking a Sr. Manufacturing Automation Engineer to join their team. As a Sr. Manufacturing Automation Engineer, you will be part of the Infectious Disease Developed Markets Business Unit supporting manufacturing processes, quality initiatives, and engineering projects. The ideal candidate will demonstrate innovative thinking, strong problem‑solving skills, and a collaborative spirit, which will align successfully in the organization.

Job Title: Sr. Manufacturing Automation Engineer

Location: Westbrook, ME

Pay Range: $57

What’s the Job?

• Support manufacturing processes by implementing engineering principles and ensuring compliance with cGMP quality and safety standards.
• Lead automation equipment upgrades, troubleshooting, and continuous improvement initiatives to enhance safety and efficiency.
• Design and execute experiments, analyze data, and present findings to cross‑functional teams for process validation and optimization.
• Create and revise technical documents, SOPs, validation protocols, and risk assessments to maintain regulatory compliance.
• Manage cross‑functional project teams, provide training, and mentor junior engineers and technicians to foster a culture of safety and continuous improvement.

What’s Needed?

• Bachelor’s degree in engineering or a related field, with 7+ years of manufacturing engineering experience.
• Proficiency in Lean Six Sigma principles, DMAIC, and structured problem‑solving methodologies.
• Experience working within ISO, FDA, or similar regulated environments, including cGMP practices.
• Strong technical skills in equipment specification, automation, troubleshooting, and process control evaluation.
• Proficiency in statistical analysis software, Microsoft Office Suite, and CAD tools.

What’s in It For Me?

• Opportunity to work in a dynamic, innovative environment focused on impactful healthcare solutions.
• Engagement in meaningful projects that drive continuous improvement and operational excellence.
• Collaborative team culture that values diversity, inclusion, and professional growth.
• Competitive pay and comprehensive benefits package.
• Chance to develop your skills and advance your career within a global organization.

Benefits Upon Completion Of Waiting Period

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• 401(k), Plus Match
• Weekly Pay