Manufacturing Engineer II

BioPharma Consulting JAD Group; Houston (TX); On-site; USD 70,000 - 95,000; Full time

Job summary

BioPharma Consulting JAD Group in Houston, TX is seeking a Manufacturing Engineer II to support our regulated manufacturing operations. You will provide engineering support to production, drive process improvements, troubleshoot equipment and process issues, and assist with quality/compliance activities.

The role requires a Bachelor's degree in Engineering and experience in a regulated environment; strong analytical, writing, and cross-functional collaboration skills are essential.

Qualifications

• Bachelor's degree in Engineering (Mechanical, Industrial, Chemical, Biomedical or related).
• Experience in regulated environments (medical device, pharmaceutical or similar) preferred.
• Familiarity with GMP/quality systems, validation and change control.

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 skills

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