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Process Improvement / Automation Engineer (Injection Molding/Blow Molding)

Full-time

Insight Global

This role will support their manufacturing facility in Oceanside, CA . The company designs and manufactures innovative laboratory products and consumables used in the biotech, pharmaceutical, and life sciences industries . Their products support cell growth, sample clarification, and analytical chemistry workflows.

Key Responsibilities

  • Identify automation and semi-automation opportunities across manufacturing operations.
  • Partner with automation integrators to design and implement scalable automation solutions.
  • Support New Product Development (NPD) by identifying automation opportunities early in the product lifecycle.
  • Lead automation projects from concept through stabilization using A3 / Project Charter methodology.
  • Manage integrator selection, scope definition, design reviews, FAT/SAT, installation, and ramp-up.
  • Establish baseline and target metrics for quality, capacity, labor, and cost improvements.
  • Collaborate with Manufacturing, Quality, and Engineering teams to ensure compliant and sustainable solutions.

Success Metrics

  • Automation projects delivered on time and within budget.
  • Measurable improvements in quality, capacity, delivery, and cost.
  • Successful integration of automation into NPD processes.
  • Long-term adoption of scalable automation solutions by operations teams.

Required Qualifications

  • Bachelor's degree in Mechanical, Electrical, Mechatronics, Manufacturing Engineering, or a related field.
  • 7+ years of automation experience in:
  • Injection molding
  • Injection blow molding
  • Blow molding environments
  • 7+ years of hands-on experience owning automation projects from:
  • Process assessment
  • Design and specification
  • Integrator management
  • Installation
  • Ramp-up and stabilization
  • 5+ years working with automation integrators and capital equipment suppliers.
  • Experience within regulated manufacturing environments such as:
  • Life Sciences
  • Medical Devices
  • Pharmaceutical Manufacturing
  • FDA/GMP/ISO-regulated industries
  • Experience with IQ/OQ/PQ validation.

Preferred Qualifications

  • Strong project management skills.
  • Experience with A3 problem-solving methodologies.
  • Hands-on manufacturing mindset.
  • Ability to influence and collaborate across cross-functional teams.
  • Strong communication skills with both technical and non-technical stakeholders.
Vacancy posted 13 hours ago
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