What are the responsibilities and job description for the Automation & Controls Engineer - Westbrook, ME position at Select Source International?
Job Title: Manufacturing Automation Engineer
Location: Westbrook, ME 04092 Onsite
Duration: 12 Month Contract with potential extension
Shift Time: 8:00 AM 5:00 PM/Monday Friday
Job Description
We are looking for a highly motivated Senior Manufacturing Automation Engineer to support manufacturing operations, automation projects, equipment upgrades, and continuous improvement initiatives within a regulated medical device environment.
Key Responsibilities
Lead automation equipment upgrades, troubleshooting, and process improvements
Drive root cause investigations, CAPA activities, and failure analysis
Support equipment validation, process characterization, and manufacturing excellence
Manage cross-functional projects and mentor engineers/technicians
Develop and maintain SOPs, validation protocols, risk assessments, and technical documentation
Ensure compliance with FDA, cGMP, ISO 13485, and quality system requirements
Qualifications
Bachelor's Degree in Engineering
7 years of manufacturing engineering experience
Experience with automation systems, process controls, and equipment troubleshooting
Lean Six Sigma / DMAIC problem-solving experience
Strong knowledge of GMP, FDA, and ISO-regulated environments preferred
Experience with validation, change management, CAPA, and continuous improvement initiatives
Location: Westbrook, ME 04092 Onsite
Duration: 12 Month Contract with potential extension
Shift Time: 8:00 AM 5:00 PM/Monday Friday
Job Description
We are looking for a highly motivated Senior Manufacturing Automation Engineer to support manufacturing operations, automation projects, equipment upgrades, and continuous improvement initiatives within a regulated medical device environment.
Key Responsibilities
Lead automation equipment upgrades, troubleshooting, and process improvements
Drive root cause investigations, CAPA activities, and failure analysis
Support equipment validation, process characterization, and manufacturing excellence
Manage cross-functional projects and mentor engineers/technicians
Develop and maintain SOPs, validation protocols, risk assessments, and technical documentation
Ensure compliance with FDA, cGMP, ISO 13485, and quality system requirements
Qualifications
Bachelor's Degree in Engineering
7 years of manufacturing engineering experience
Experience with automation systems, process controls, and equipment troubleshooting
Lean Six Sigma / DMAIC problem-solving experience
Strong knowledge of GMP, FDA, and ISO-regulated environments preferred
Experience with validation, change management, CAPA, and continuous improvement initiatives
Salary : $55 - $60