Manufacturing Engineer II

Biopharma-Consulting-Jad-Group; Houston (TX); On-site; USD 75,000 - 105,000; Full time

Job summary

Biopharma-Consulting-Jad-Group is seeking a Manufacturing Engineer II to support manufacturing operations in a regulated facility in Houston, TX. The role focuses on providing engineering support to production, driving process improvements, troubleshooting equipment and process issues, and supporting quality/compliance activities.

Key responsibilities include supporting day-to-day engineering, implementing process improvements to boost yield and efficiency, handling investigations and CAPAs, and

Qualifications

• Bachelor's degree in Engineering required.
• Experience in a regulated manufacturing environment preferred (medical device/pharma).
• Knowledge of GMP/quality systems, validation and change control preferred.
• Experience with root cause analysis and problem-solving tools.

Responsibilities

• Provide day-to-day engineering support to manufacturing lines, including equipment and process troubleshooting.
• Identify and implement process improvements to increase yield, efficiency and product quality.
• Support nonconformances, investigations, root cause analysis and CAPAs.
• Author and update manufacturing procedures, work instructions and technical documentation.
• Support change controls, equipment qualification and process validation activities.
• Work cross-functionally with Production, Quality, Maintenance and other Engineering teams.

Skills

Analytical thinking

Troubleshooting

Technical writing

Education

Bachelor's degree in Engineering

Job description

We are seeking a Manufacturing Engineer II to support manufacturing operations at a regulated manufacturing facility in Houston, Texas. This role provides engineering support to production, driving process improvements, troubleshooting equipment and process issues, and supporting quality and compliance activities.

Key Responsibilities

• Provide day-to-day engineering support to manufacturing lines, including equipment and process troubleshooting.
• Identify and implement process improvements to increase yield, efficiency and product quality.
• Support nonconformances, investigations, root cause analysis and CAPAs.
• Author and update manufacturing procedures, work instructions and technical documentation.
• Support change controls, equipment qualification and process validation activities.
• Work cross-functionally with Production, Quality, Maintenance and other Engineering teams.

Education

• Bachelor's degree in Engineering (Mechanical, Industrial, Chemical, Biomedical or related)

Preferred Qualifications

• Manufacturing engineering experience in a regulated environment (medical device, pharmaceutical or similar)
• Working knowledge of GMP/quality system requirements, validation and change control
• Experience with root cause analysis and problem-solving tools

Key Skills

• Strong analytical and troubleshooting skills
• Clear technical writing and communication
• Ability to manage multiple priorities in a production environment

• Contract position: approximately 24 months, starting October 2026
• Shift: Full-time, 40 hours/week
• On-site in Houston, Texas