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

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.Considering making an application for this job Check all the details in this job description, and then click on Apply.Key ResponsibilitiesIdentify 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 MetricsAutomation 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 QualificationsBachelor's degree in Mechanical, Electrical, Mechatronics, Manufacturing Engineering, or a related field.7+ years of automation experience in:Injection moldingInjection blow moldingBlow molding environments7+ years of hands-on experience owning automation projects from:Process assessmentDesign and specificationIntegrator managementInstallationRamp-up and stabilization5+ years working with automation integrators and capital equipment suppliers.Experience within regulated manufacturing environments such as:Life SciencesMedical DevicesPharmaceutical ManufacturingFDA/GMP/ISO-regulated industriesExperience with IQ/OQ/PQ validation.Preferred QualificationsStrong project management skills.Experience with A3 problem-solving methodologies.Hands-on manufacturing mindset.Ability to influence and collaborate across cross-functional teams. xhyhwjd Strong communication skills with both technical and non-technical stakeholders.

Vacancy posted 3 days ago
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