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6 дней назад

Sr Manager, Industrial Engineering & Process Optimization (Biotechnology)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Sr Manager, Industrial Engineering & Process Optimization (Biotechnology): Driving continuous improvement across high-throughput manufacturing operations with an accent on capacity expansion, turnaround-time reduction, first-pass yield, and resource utilization. Focus on analyzing production bottlenecks, building ROI models for process and automation changes, and implementing compliant improvements using industrial engineering methods in ISO 13485 and GxP-regulated environments.

Location: Onsite in Wilsonville, Oregon, USA; the posting header also lists Portland, Oregon.

Company

hirify.global develops silicon-based DNA synthesis technology for applications in healthcare, agriculture, industrial chemicals, and data storage.

What you will do

  • Analyze manufacturing performance data to identify capacity constraints, turnaround-time bottlenecks, quality losses, and labor inefficiencies.
  • Lead root cause analysis and improvement initiatives to reduce rework, scrap, defects, and reprocessing.
  • Design and validate process changes using time-motion studies, line balancing, capacity modeling, value stream mapping, and DOE.
  • Develop improvement pipelines, business cases, ROI models, and capital equipment proposals.
  • Partner with Manufacturing, Operations, Quality, Automation Engineering, and Workforce Planning on scalable process, automation, and staffing improvements.
  • Track OEE, first-pass yield, cycle time, and cost per unit, and present roadmaps and results to senior leadership.

Requirements

  • Bachelor’s or Master’s degree in Industrial Engineering, Mechanical Engineering, Manufacturing Engineering, or a related technical field.
  • 8–12+ years of progressive experience in industrial engineering, continuous improvement, or manufacturing process optimization.
  • 3–5+ years of supervisory, management, or cross-functional team leadership experience.
  • Hands-on experience in ISO 13485 or GxP-regulated environments, including compliant change control and documentation.
  • Expertise in OEE, Cpk, takt time, cost-per-unit modeling, time-motion studies, line balancing, capacity modeling, and value stream mapping.
  • Ability to influence cross-functional stakeholders without direct authority over manufacturing execution.

Nice to have

  • Experience in high-throughput biomanufacturing, biotechnology, or life science manufacturing.
  • Experience leading complex, multifunctional process optimization or automation initiatives from diagnosis through execution.

Culture & Benefits

  • Work within an engineering organization focused on operational excellence and scalable manufacturing improvements.
  • Collaborate closely with Manufacturing, Operations, Quality, Automation Engineering, and Workforce Planning.
  • Support applications of DNA synthesis technology across healthcare, agriculture, industrial chemicals, and data storage.

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