Sr. Manufacturing Engineer

Job Title: Sr. Manufacturing Engineer

Location: 5 Bradley Drive, Westbrook, ME 04092

Duration: 3 Months

Work Arrangement: 100% Onsite

Position Overview

We are seeking a Senior Manufacturing Automation Engineer to support manufacturing operations within the Infectious Disease Developed Markets Business Unit based in Scarborough, Maine. This role focuses on optimizing manufacturing processes, driving quality and cost-efficiency initiatives, and ensuring compliance with cGMP, FDA, and ISO standards.

Key Responsibilities

• Ensure compliance with company policies, procedures, and regulatory requirements (FDA, ISO, cGMP).
• Support manufacturing operations, process improvements, and cost-saving initiatives.
• Lead automation equipment upgrades related to safety, obsolescence, and continuous improvement.
• Troubleshoot equipment issues involving machine logic, electromechanical systems, and process controls.
• Perform root cause analysis and implement corrective and preventive actions (CAPA).
• Conduct risk assessments and Failure Modes and Effects Analysis (FMEA).
• Lead design of experiments (DOE), validation activities, testing, and data analysis.
• Develop and maintain manufacturing documentation including SOPs, validation protocols, and specifications.
• Drive implementation of new methods, materials, and technologies to improve efficiency and quality.
• Analyze equipment performance and recommend process improvements.
• Lead cross-functional teams and manage project activities and timelines.
• Provide technical training and mentorship to engineers and technicians.
• Support change management initiatives and participate in site strategy planning.
• Ensure effective collaboration with internal teams, vendors, and stakeholders.

Required Qualifications

• Bachelor’s degree in Engineering or equivalent experience.
• 7+ years of experience in a manufacturing environment.
• Experience with Lean Six Sigma methodologies (DMAIC or similar).
• Strong understanding of change management principles.

Preferred Qualifications

• Experience working in regulated environments (FDA, ISO, GMP, ISO 13485).
• Familiarity with statistical analysis tools.
• Proficiency in Microsoft Office (Excel, PowerPoint, Power BI).

Core Competencies

• Strong analytical and problem-solving skills.
• Ability to manage multiple priorities effectively.
• Excellent verbal and written communication skills.
• Self-motivated with a proactive and results-driven approach.
• Strong teamwork and collaboration skills.

Technical Skills

• Knowledge of fabrication and manufacturing processes (CNC, machining, welding).
• Ability to interpret technical drawings and engineering instructions.
• Experience with CAD and manufacturing software.
• Understanding of statistical methods and quality standards.
• Experience with materials testing and performance evaluation.

Consultants Eligible Benefits Upon Waiting Period:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.