Top Process Engineer Jobs

Lead startup, development, and optimization of PVD/CVD processes for DRAM manufacturing. Improve yield, reduce cost, resolve production issues, drive SPC improvements, and collaborate with equipment and integration teams to meet project milestones.

Develop, start up, and optimize wet etch processes for DRAM manufacturing to improve yield, reduce defects and cost. Collaborate with equipment and integration engineers, drive SPC improvements, manage projects to close yield/production gaps, and apply data science/AI tools to improve workflows.

Leads HR process re-engineering and operational improvement initiatives by analyzing current-state workflows, identifying root causes, designing simplified future-state processes, and strengthening controls. Facilitates stakeholder workshops, applies Lean methodologies, documents process requirements, measures benefits, and evaluates AI or automation opportunities. Partners with Technology, AI, Risk, Controls, process owners, and project managers through implementation and benefit realization.

Process/Manufacturing Engineer responsible for production efficiency, equipment and line industrialization, process validation, lean improvement, cycle-time reduction, supplier coordination, equipment acceptance, production support, standardization, and safety and environmental compliance in a high-speed automotive manufacturing environment.

Develops and continuously improves aerospace manufacturing processes involving composites, machining, rubber layup, molding, bonding, coatings, and complex assemblies. Supports production operations, investigates root causes, creates engineering and planning documentation, authors work instructions, applies SPC, troubleshoots tooling and facility issues, and implements process, equipment, and quality improvements. The role also supports tooling qualification and presents technical information to leadership and customers.

Provides process engineering support for GMP oligonucleotide manufacturing, including process troubleshooting, optimization, lifecycle management, capital projects, equipment design, commissioning, qualification, validation, and continuous improvement. Collaborates with manufacturing, quality, safety, development, and project teams; supports technical transfers, scale-up, regulatory activities, CAPAs, change controls, audits, process safety, and compliant pharmaceutical facility operations.

Supports downstream biotherapeutics process development through chromatography, harvest, ultrafiltration/diafiltration, and viral clearance experiments across micro, bench, and pilot scales. Maintains laboratory equipment and electronic records, performs basic data analysis, prepares technical summaries, follows quality and safety procedures, and contributes to workflow improvements and small development projects under supervision.

Supports downstream biotherapeutics process development through chromatography, harvest, UF/DF, viral clearance, and purification experiments across micro, bench, and pilot scales. Maintains laboratory equipment, documents work in electronic laboratory notebooks, analyzes data, prepares technical summaries, follows quality and safety procedures, and contributes to process optimization and continuous improvement under close supervision.

Supports production safety, quality, and delivery while leading equipment qualification, customer-facing process development, engineering change control, audits, risk assessments, process control plans, SPC and MSA programs, nonconformance disposition, and technical training. The role develops chemical, mechanical, and robotic processes for semiconductor parts cleaning and surface enhancement, requiring work in chemical, hazardous, noisy, and physically demanding environments.

Lead and supervise process engineering teams on capital projects, delivering designs, estimates, schedules, and specifications. Establish design criteria, perform detailed calculations and drawings, ensure safety and code compliance, review vendor data, and coordinate interdisciplinary work. Mentor junior engineers, support proposals and client presentations, and manage project scope, budget, and schedule. Travel as required.

Engineering internship supporting PCB manufacturing through production, process and yield improvement projects. Responsibilities include qualification experiments, documentation, data formatting, statistical failure analysis, and process-related projects. Candidates will apply structured problem-solving, data analysis, procedure writing, and manufacturing engineering knowledge while pursuing an engineering bachelor’s degree.

Develops, optimizes, validates, and deploys manufacturing, test, automation, and production equipment. Responsibilities include equipment procurement and commissioning, process analysis, root cause investigation, corrective actions, documentation, Lean and Six Sigma improvement, project scheduling, stakeholder coordination, and performance validation. The role manages multiple deployment and process improvement projects while ensuring safety, quality, efficiency, and operational continuity.

Lead TOPCon solar cell process engineering across tunnel oxide, polysilicon deposition, diffusion, passivation, and metallization. Drive process stability, yield improvement, root cause analysis, process control, documentation, tool readiness, technology transfer, and qualification. Mentor engineers and collaborate with equipment, metrology, quality, R&D, and device engineering teams to scale advanced cell technology into high-volume manufacturing.

Support safe and efficient smelter operations by monitoring process performance, analyzing operational data, resolving process issues, and recommending improvements. The role contributes to equipment and process design, asset optimization, technical specifications, smaller engineering projects, reporting, and technical support for operations, maintenance, contractors, and project teams.

Develops, validates, and optimizes automated assembly processes from commissioning through production. Owns PLC, robotics, servo, vision, safety, and material-handling performance; leads equipment acceptance, installation, commissioning, troubleshooting, production launches, and supplier actions. Improves throughput, uptime, cycle time, reliability, and quality while maintaining controls standards, documentation, backups, contingency plans, and training. Partners with manufacturing, maintenance, quality, IT/OT, EHS, and suppliers to ensure stable production flow.

Leads manufacturing process engineering for turbine engine components, including five-axis machining with milling machines, lathes, and grinders. Provides shop-floor support, technical leadership, training, process troubleshooting, root cause analysis, tooling and equipment control, and validation of new products and processes. Develops moderate-impact project plans, supports continuous improvement, and works primarily on second shift.

Provides technical leadership for pharmaceutical packaging launches and continuous improvement. Designs production lines, layouts, tooling, and equipment; prepares engineering, validation, and capital equipment documentation; leads commissioning, FAT/SAT, CAPA, and Lean Six Sigma initiatives; analyzes performance metrics and reduces defects, waste, and variability. Supports production, maintenance, quality, validation, purchasing, sales, customers, and vendors while ensuring compliance with PCI, cGMP, and GCP requirements.

Leads end-to-end process engineering for aseptic vial and syringe filling systems in a new cGMP biotherapeutic manufacturing facility. Responsibilities include equipment specification and vendor selection, facility integration, design, commissioning, qualification, start-up, technical issue resolution, and cross-functional project leadership. The role ensures regulatory compliance with FDA cGMPs and EU Annex 1 while partnering with vendors, contractors, and internal teams to deliver high-performing filling systems.

Supports the design and documentation of manufacturing facilities, equipment, infrastructure, and critical utility systems. Performs basic engineering calculations, process modeling, material and energy balances, equipment sizing, and fluid or heat transfer analyses under supervision. Develops process flow diagrams, P&IDs, equipment lists, datasheets, utility summaries, and related design documents. Collaborates with multidisciplinary teams, supports construction documentation and administration, and may conduct site observations and assist field installation teams.

Develops and qualifies materials and manufacturing processes for aerospace and defense hardware. Responsibilities include material selection, process planning, drawing reviews, laboratory testing, data analysis, failure investigations, root cause and corrective action, supplier requirement flow-down, and cross-functional support for design and production. The role works across offices, laboratories, production floors, and cleanrooms, requiring aerospace materials experience and a DoW Interim Secret clearance.

Develops and qualifies materials and manufacturing processes for aerospace and defense hardware. Reviews drawings, selects materials, analyzes laboratory data, performs failure investigations, and leads root-cause and corrective-action activities. The role supports design, production, suppliers, and subcontractors by authoring requirements and verifying compliance. Work occurs onsite across office, laboratory, production, cleanroom, and outdoor environments, with occasional travel between Colorado campuses and other locations. A DoW Interim Secret clearance is required to start and maintain employment.

Supports powertrain manufacturing quality and process robustness through PFMEAs, Control Plans, root cause analysis, corrective actions, launch and warranty reviews, audits, training, and continuous improvement. Collaborates with global quality, plant, product development, and engineering teams to resolve concerns and improve Ford’s Quality Operating System. Requires plant manufacturing and quality experience, with travel to powertrain plants as needed.

Provides technical leadership and daily support for specialty chemical manufacturing operations. Optimizes chemical processes, troubleshoots equipment and yield issues, investigates quality events, implements CAPAs, and supports safety and regulatory compliance. Leads capital improvement projects from design through commissioning, develops P&IDs and equipment specifications, and maintains SOPs and batch documentation. Collaborates with manufacturing, maintenance, quality, EHS, management, and union personnel in an onsite facility.

Leads enterprise process analysis, redesign, and transformation initiatives across business functions. Uses Lean, Six Sigma, DMAIC, value-stream mapping, systems engineering, process mining, and automation methods to improve cycle time, cost, quality, compliance, and capacity. Facilitates stakeholders, defines requirements and governance, establishes performance metrics, supports technology implementation, and presents recommendations to leadership. Provides mentorship and subject matter expertise without formal people-management responsibility.

Supports Manufacturing Science and Technology activities in a GMP-regulated manufacturing environment, primarily conducting Out-of-Specification investigations. Reviews batch records, process data, equipment logs, and analytical results; develops investigation findings and conclusions; and collaborates with Quality, Manufacturing, Engineering, and management. The role requires technical writing, troubleshooting, data analysis, GMP documentation familiarity, and cross-functional communication. Pharmaceutical or biopharmaceutical experience and cell therapy manufacturing knowledge are preferred.