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Abbott · 1 day ago

Manufacturing Process Engineer

Scottsdale, AZ

Full-time

Onsite

Entry Level

$61K/yr - $123K/yr

1+ years exp

Abbott is a global healthcare leader that helps people live more fully at all stages of life. The Manufacturing Process Engineer is responsible for implementing and maintaining high volume manufacturing processes, ensuring compliance with medical device manufacturing requirements, and conducting process capability analysis to improve product performance.

BiotechnologyEmergency MedicineGeneticsHealth CareHealth DiagnosticsManufacturingMedicalMedical DeviceNutritionPharmaceutical

Responsibilities

As the Experienced professional in the Medical Device Manufacturing Process Sub-Function, possesses well developed skills in implementing and maintaining high volume manufacturing processes

Serve as the primary process owner for several PCB manufacturing processes, including Solder, Epoxy Dispense, Wirebond, Underfill, Laser Processing, and Mechanical Routing

Establish and maintain robust, compliant, and validated processes that meet medical device manufacturing requirements

Develop and maintain process documentation, including work instructions, standard work, control plans, PFMEAs, and equipment settings

Conduct and document process capability analysis (Cp/Cpk) and implement actions to improve reliability and product performance

Own the lifecycle of process equipment : reflow ovens, dispensers, pick‑and‑place modules, wirebonders, underfill systems, lasers, mechanical routers, etc

Define equipment requirements, support vendor evaluations, lead installations, and oversee equipment validation (IQ/OQ/PQ)

Collaborate with maintenance on PM schedules, calibration, uptime tracking, and tooling readiness

Evaluate and qualify all process materials, including solder paste, flux, epoxy/adhesives, underfill chemistries, wirebond materials, and cleaning solvents

Monitor daily yield, scrap, and defect trends; drive root cause investigation, CAPA activities, and long‑term corrective actions

Services, troubleshoots, and solves engineering problems with processes or equipment already in operation

Generate and execute process validation protocols (IQ/OQ/PQ, PPQ) in alignment with medical device regulatory expectations

Provide manufacturability feedback to R&D on PCB layout, component spacing, bond pad design, solder joint access, and material compatibility

Qualification

Medical Device ManufacturingProcess ValidationProcess DocumentationPCB Manufacturing ProcessesEquipment ValidationRoot Cause AnalysisTroubleshootingCollaboration

Required

Associates Degree (± 13 years)

Minimum 1 year of experience in Medical Device Manufacturing Process

Well developed skills in implementing and maintaining high volume manufacturing processes

Ability to serve as the primary process owner for several PCB manufacturing processes, including Solder, Epoxy Dispense, Wirebond, Underfill, Laser Processing, and Mechanical Routing

Experience in establishing and maintaining robust, compliant, and validated processes that meet medical device manufacturing requirements

Ability to develop and maintain process documentation, including work instructions, standard work, control plans, PFMEAs, and equipment settings

Experience in conducting and documenting process capability analysis (Cp/Cpk) and implementing actions to improve reliability and product performance

Ability to own the lifecycle of process equipment: reflow ovens, dispensers, pick-and-place modules, wirebonders, underfill systems, lasers, mechanical routers, etc

Experience in defining equipment requirements, supporting vendor evaluations, leading installations, and overseeing equipment validation (IQ/OQ/PQ)

Ability to collaborate with maintenance on PM schedules, calibration, uptime tracking, and tooling readiness

Experience in evaluating and qualifying all process materials, including solder paste, flux, epoxy/adhesives, underfill chemistries, wirebond materials, and cleaning solvents

Ability to monitor daily yield, scrap, and defect trends; drive root cause investigation, CAPA activities, and long-term corrective actions

Experience in servicing, troubleshooting, and solving engineering problems with processes or equipment already in operation

Ability to generate and execute process validation protocols (IQ/OQ/PQ, PPQ) in alignment with medical device regulatory expectations

Ability to provide manufacturability feedback to R&D on PCB layout, component spacing, bond pad design, solder joint access, and material compatibility