Manufacturing Engineer II

Posted 3 Days Ago
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Houston, TX, USA
In-Office
Entry level
Biotech • Pharmaceutical
The Role
Provides day-to-day engineering support for manufacturing lines, troubleshooting equipment and processes while improving yield, efficiency, and product quality. Supports nonconformance investigations, root cause analysis, CAPAs, change controls, equipment qualification, process validation, and quality compliance. Authors manufacturing procedures, work instructions, and technical documentation in a regulated facility.
Summary Generated by Built In

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.

Requirements
  • 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.

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

Skills Required

  • Bachelor's degree in Engineering, such as Mechanical, Industrial, Chemical, Biomedical, or a related field.
  • Manufacturing engineering experience in a regulated environment such as medical device or pharmaceutical manufacturing.
  • Knowledge of GMP and quality systems.
  • Knowledge of validation and change control.
  • Strong analytical and troubleshooting skills.
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The Company
HQ: Cambridge, MASSACHUSETTS
39 Employees
Year Founded: 2010

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.

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