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.
Requirements
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
Benefits
- Contract position: approximately 24 months, starting October 2026
- Shift: Full-time, 40 hours/week
- On-site in Houston, Texas
Skills Required
- Bachelor's degree in Engineering, such as Mechanical, Industrial, Chemical, Biomedical, or a related discipline
- Manufacturing engineering experience in a regulated environment, such as medical device or pharmaceutical manufacturing
- Working knowledge of GMP and quality system requirements
- Experience with validation and change control
- Experience with root cause analysis and problem-solving tools
- Strong analytical and troubleshooting skills
- Clear technical writing and communication skills
- Ability to manage multiple priorities in a production environment
What We Do
BioPharma Consulting JAD Group provides a complete portfolio of technical support and solutions for the FDA regulated industry. We deliver solutions with a flexible cost effective approach to meet your company’s needs. BPC JAD group is a company created to help our customers bridge the gap between their business strategy and results. Our mission is to help our clients succeed by partnering with them and providing value added business solutions on the validation, engineering and compliance fields. We will carry out our mission by creating a long-term partnership with our customers and provide reliable and cost effective technical solutions. BPC JAD Group objective is to deliver reliable tailored solutions; from providing consultation to becoming part of your staff. We will develop customized frameworks to help our customers unlock the hidden value in their plants, facilities, equipment and people with an optimal integration of resources regulations and technology.
