Manufacturing Engineer I

Abbott; Plano (TX); On-site; USD 38,572 - 52,348; Full time

Benefits offered by this job

Medical Plan

Dental Plan

Vision Plan

Health Savings Account

Flexible Spending Accounts

Life Insurance

Disability Insurance

401(k)

Job summary

Abbott is seeking a Manufacturing Engineer I for a 5-month, 100% onsite assignment in Plano, TX. You will implement and validate new equipment and processes within the IQ/OQ/PQ framework and work with Quality, Production, and R&D to ensure compliant manufacturing operations.

The role involves troubleshooting production issues, monitoring yield and scrap data, and driving process improvements in a regulated environment. 0–3 years of relevant experience is expected.

Qualifications

• 0–3 years of relevant experience in manufacturing.
• IQ/OQ/PQ validation knowledge and FDA/ISO awareness.
• Experience with data analysis and process improvement.

Responsibilities

• Implement and validate new equipment and processes (IQ/OQ/PQ).
• Troubleshoot manufacturing and equipment-related issues.
• Monitor and analyze yield, scrap, and defect data.
• Drive continuous improvement initiatives.
• Collaborate with cross-functional teams to ensure smooth operations.
• Document findings and maintain compliance with FDA/ISO standards.

Skills

Technical problem-solving

Process validation (IQ/OQ/PQ)

Data analysis

Communication skills

Regulatory awareness

Education

Bachelor’s degree in Mechanical Engineering / Industrial Engineering / Electrical Engineering / Chemical Engineering / Bioengineering

Job description

Title: Manufacturing Engineer I

Location: Plano, TX

Duration: 5 Month Assignment

100% Onsite

Summary

The Manufacturing Engineer I supports daily manufacturing operations by implementing new equipment and processes using the IQ/OQ/PQ validation framework. Responsibilities include troubleshooting production issues, monitoring yield metrics, investigating scrap and defects, and driving continuous improvement initiatives. The engineer will work closely with cross-functional teams such as Quality, Production, and R&D to ensure compliant and efficient manufacturing processes.

Key Responsibilities

• Implement and validate new equipment and processes (IQ/OQ/PQ).
• Troubleshoot manufacturing and equipment-related issues.
• Monitor and analyze yield, scrap, and defect data.
• Drive continuous improvement initiatives.
• Collaborate with cross-functional teams to ensure smooth operations.
• Document findings and maintain compliance with FDA/ISO standards.
• Required Experience: 0–3 years of relevant experience

Top 5 Key Skills

• Technical problem-solving
• Process validation knowledge (IQ/OQ/PQ, FDA/ISO)
• Data analysis (yield, scrap, process metrics)
• Strong communication skills
• Attention to detail in regulated environments

Preferred Experience

• Internship or co-op in regulated manufacturing (medical devices/pharma)
• Exposure to Lean Manufacturing or Six Sigma
• Experience with statistical tools (e.g., Minitab, JMP)
• Familiarity with ERP or MES systems
• Hands-on experience with equipment installation or automation

Required Education

• Bachelor’s degree in Mechanical Engineering (preferred), Industrial Engineering, Electrical Engineering, Chemical Engineering, or Bioengineering

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)