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Vantage

Manufactures naturally derived specialty ingredients

Production Engineer

Process EngineeringConfirmed live in the last 24 hours
Full-timeEnglewood, OH, USA

About the Job

Requirements

  • A Bachelor of Science in Chemical, Mechanical, or Industrial Engineering is required.
  • At least 2 years of experience in a manufacturing environment, including at least 1 year in process or production engineering, is required.
  • Strongly preferred: pharmaceutical or active pharmaceutical ingredient manufacturing experience, including current good manufacturing practice, batch records, deviations and corrective and preventive actions, change control, and validation.
  • Experience in personal care, cosmetics, nutraceutical, food, or specialty chemical manufacturing is valued.
  • Hands-on experience with one or more of liquid or powder blending, encapsulation, milling or size reduction, spray congealing or spray drying, extrusion, or packaging/downpacking operations.
  • Strongly preferred: experience implementing manufacturing automation, such as material handling, dispensing, controls, or packaging automation.
  • Lean or Six Sigma training or certification at Green Belt level or higher is a plus.
  • Ability to coach, train, and influence hourly teams and supervisors without direct authority, and build standard work that is followed.
  • Structured, data-driven root cause troubleshooting skills, including statistical process control, trend analysis, and designed trials.
  • Practical knowledge of powder and liquid processing, including mixing, particle size reduction, heat transfer, and the effects of process conditions on product quality and stability.
  • Ability to identify appropriate automation opportunities and develop a sound business case for them.
  • Working knowledge of programmable logic controllers, human-machine interfaces, controls, material handling equipment, mechanical systems, utilities, and reliability practices; experience with automation integrators and equipment vendors is a plus.
  • Ability to manage multiple priorities and adjust focus to urgent safety, quality, or equipment issues while maintaining longer-term improvement and project work.
  • Clear communication across Production, Maintenance, Quality, Planning, Research and Development, and with customers when needed.
  • Proficiency with Excel and data analysis tools; enterprise resource planning and manufacturing execution system experience is a plus.
  • Ability to work on-site five days per week and provide periodic off-shift or weekend support as production needs require.

Responsibilities

  • Monitor production processes daily across blending, encapsulation, milling, spray congealing, extrusion, and downpacking; learn each process, review batch records, process parameters, yields, cycle times, and in-process results, and respond to deviations before they affect product quality or the schedule.
  • Collect real-life production data through observation, time studies, downtime and deviation records, and operator input; maintain and regularly review with site leadership a prioritized list of improvement opportunities ranked by safety, quality, and productivity impact.
  • Specify and run plant trials, partnering with Research and Development and technical service, to establish and tighten process parameters for safety, quality, throughput, and product stability; translate results into updated batch instructions, standard operating procedures, and operating windows.
  • Lead structured root cause analyses, including 5 Whys, fishbone analysis, and failure mode and effects analysis, on equipment failures, process upsets, and batch deviations; partner with Maintenance on preventive and predictive maintenance and critical spares, and track and trend downtime by cause to eliminate repeat events.
  • Work with Planning and production supervision to remove schedule execution constraints, including changeovers, cleaning, material staging, equipment availability, and staffing.
  • Eliminate sources of rework, reprocessing, off-specification material, and documentation errors through robust process controls, error-proofing, and clear work instructions.
  • Learn manual operations firsthand alongside operators, including material charging, bag dumping, weighing, material handling, and downpacking; map processes, measure labor content and variability, and identify safety, ergonomic, and quality risks from manual handling.
  • Identify and implement automation solutions such as automated material handling and transfer, powder conveying, bulk bag unloading, automated weighing and dispensing, recipe-driven controls, and packaging automation; build business cases and oversee specification, vendor selection, installation, and startup.
  • Develop standard work, visual work instructions, and hands-on operator training for new and existing processes; involve operators in improvement and automation design and support them through changes to their roles.
  • Support deviation investigations, corrective and preventive actions, and change control with Quality; ensure processes meet current good manufacturing practice expectations for active pharmaceutical ingredient manufacturing, including ICH Q7 and 21 CFR 210/211, and personal care ingredient quality standards.
  • Support customer complaint investigations and connect process performance to customer outcomes; monitor process capability on critical quality attributes to maintain consistent, stable products from lot to lot.
  • Facilitate actions across Production, Maintenance, Quality, Planning, and outside vendors by assigning owners and timelines, removing roadblocks, and following through until improvements are implemented and sustained.
  • Establish and maintain production key performance indicators, including unplanned downtime, overall equipment effectiveness, schedule attainment, Right First Time, On Time In Full, and customer complaints; review them in daily tier meetings and monthly operations reviews.
  • Apply Lean and Six Sigma tools, including standard work, 5S, SMED, statistical process control, and value stream mapping, to improve capacity, cost, and consistency.
  • Participate in process hazard analysis and hazard and operability reviews and Management of Change, with particular attention to powder handling, dust hazards, and ergonomic risks from manual operations.
  • Scope, justify, and execute capital and expense projects, including automation projects, to improve safety, reliability, capacity, and quality or reduce manual labor; support commissioning, startup, and operator training on new or modified equipment, and work with Finance on budgeting and project close-out.

Desired Qualifications

  • Experience with automation integrators and equipment vendors.
  • Enterprise resource planning and manufacturing execution system experience.
  • Lean or Six Sigma training or certification at Green Belt level or higher.
  • Experience in personal care, cosmetics, nutraceutical, food, or specialty chemical manufacturing is valued.
  • Pharmaceutical or active pharmaceutical ingredient manufacturing experience, including current good manufacturing practice, batch records, deviations and corrective and preventive actions, change control, and validation, is strongly preferred.
  • Experience implementing automation in a manufacturing environment, such as material handling, dispensing, controls, or packaging automation, is strongly preferred.

About the Company

Vantage

Manufactures naturally derived specialty ingredients

Vantage Specialty Chemicals makes naturally derived specialty ingredients for personal care, food, consumer goods, and industrial uses. It operates four units—Personal Care, Performance Materials, Oleochemicals, and Foods—and offers over 2,000 products like fatty acids, emulsifiers, and cosmetic ingredients. It uses a vertically integrated model (notably in jojoba) that controls the supply chain from farming to finished formulations, ensuring transparency and sustainable practices. Its goal is to supply high-quality, reliably sourced ingredients worldwide, supporting customers in safe, effective product formulations while growing through strategic acquisitions and a global network.

Company size
501-1,000
Company stage
Debt Financing
Total funding
$900M
Headquarters
Deerfield, IL
Founded
2008

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