Manufacturing Engineer II

BioPharma Consulting JAD Group; Houston (TX); On-site; USD 70,000 - 90,000; Full time

Job summary

BioPharma Consulting JAD Group in Houston, TX is seeking an engineer to keep production running and improve processes at a regulated manufacturing facility. You will troubleshoot equipment and processes on the manufacturing lines and support quality and compliance activities.

The role focuses on yield and efficiency improvements, GMP-compliant documentation, and participation in change controls and validations. Start is immediate; contract lasting 24 months with possible extension.

Qualifications

• Requires a Bachelor's in Engineering.
• Experience in regulated manufacturing environments preferred.
• GMP/quality systems, validation and change control knowledge.
• Strong analytical and troubleshooting abilities.

Responsibilities

• Provide day-to-day engineering support to manufacturing lines, including equipment and process troubleshooting.
• Identify and implement improvements to yield, efficiency and product quality.
• Support nonconformances, investigations, root cause analysis and CAPAs.
• Author manufacturing procedures, work instructions and technical documentation.
• Support change controls, equipment qualification and process validation.

Skills

Analytical skills

Troubleshooting

Education

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

Job description

Keep production running and improving at a regulated manufacturing facility in Houston, Texas. You will be the go-to engineer for the manufacturing lines: troubleshooting, process improvements, and quality and compliance support.

What you'll do

• Provide day-to-day engineering support to manufacturing lines, including equipment and process troubleshooting.
• Identify and implement improvements to yield, efficiency and product quality.
• Support nonconformances, investigations, root cause analysis and CAPAs.
• Author manufacturing procedures, work instructions and technical documentation.
• Support change controls, equipment qualification and process validation.

• Bachelor's degree in Engineering (Mechanical, Industrial, Chemical, Biomedical or related).
• Manufacturing engineering in a regulated environment (medical device, pharmaceutical or similar) preferred.
• GMP/quality systems, validation and change control.
• Strong analytical and troubleshooting skills.

• Contract: 24 months, with possible extension
• Shift: Full-time, 40 hours/week
• Start: Immediate