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Senior Manufacturing Automation Engineer

Job in Westbrook, Cumberland County, Maine, 04092, USA
Listing for: Iconma
Full Time position
Listed on 2026-07-01
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer
Job Description & How to Apply Below

Senior Manufacturing Automation Engineer

Our client, a medical device and healthcare company, is looking for a Senior Manufacturing Automation Engineer for their Westbrook, ME location.

Responsibilities:
  • Carries out duties in compliance with established business policies and procedures.
  • Demonstrates commitment to the development, implementation and effectiveness of applicable Quality Processes as per ISO, FDA, and other regulatory agencies.
  • Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices.
  • Responsibility to understand and maintain awareness of the quality consequences which may occur from the improper performance of their specific job.
  • Support department by performing related tasks as requested.
  • Responsible for equipment specification, acquisition, and implementation.
  • Leads automation equipment upgrade efforts related to safety, obsolescence, and continuous improvement initiatives.
  • Evaluates machine logic, electromechanical and process controls to troubleshoot equipment and drives to resolution.
  • Leads teams to identify root cause of manufacturing failures using structured problem solving.
  • Applies root cause fixes to prevent recurrence.
  • Conducts failure modes and effects analysis and evaluates manufacturing equipment risk.
  • Completes complex projects based on comprehensive knowledge of manufacturing equipment and processes.
  • Leads design of experiments, validation, completion of testing and analysis of data.
  • Presents data to cross functional teams.
  • Drives implementation of new methods or materials for continual improvement of quality and efficiency.
  • Analyzes current equipment for process suitability and provides detailed plans for improvement.
  • Creates and revises manufacturing documents, specifications, standard operating procedures (SOPs), safety instructions, validation protocols, risk assessments, and procedures and other technical documents to ensure compliant, efficient, and safe procedures.
  • Leads other engineers and technicians in developing solutions and improvements in materials, equipment, and process as necessary in addition to ensuring continual improvement, safety, and compliance.
  • Manages cross functional project teams and coordinate activities.
  • Provides training and process expertise for product processing in specific areas such as process development, tooling development, documentation, cleaning protocol, process characterization and validation.
  • Initiates and leads to resolution of Quality Incidents and CAPA.
  • Participates in teams as necessary and mentors junior engineers and maintenance technicians to ensure continual improvement, safety, and compliance.
  • Considers safety, ergonomic, maintenance, and operator impact on manufacturing design.
  • Interacts with the local Project Management Office on milestones and project status updates.
  • Participates in site strategy meetings and planning.
  • Leads change through Agile PDM.
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
Requirements:
  • Basic qualifications | education:
  • Bachelor's degree (BS) in engineering or equivalent combination of education and experience.
  • 7+ years engineering experience in a manufacturing environment
  • Experience in the application of lean six sigma principles and the DMAIC approach or a similar structured problem-solving system.
  • Proficiency in change management principles and processes.
  • Preferred qualifications:
  • Prior experience working in a company operating under ISO, FDA, or similar quality systems or regulations.
  • Experience working in a GMP, FDA, ISO and USDA regulated environment.
  • Experience in cGMP and ISO 13485 regulations and practices.
  • Experience in statistical analysis software.
  • Experience in Microsoft Suites software. (Microsoft Excel, PowerPoint, Power BI, etc.)
  • General competencies:
  • Innovative Thinking:
    Independently generates new, creative, and…
Position Requirements
10+ Years work experience
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