Process Engineer

{
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  "source_hash": "ad9ad32561c3cf80abd7c4ea0ce027b2eb3c2bbcacef1fac5d8bc09e30f52f1b",
  "last_changed_at": "2026-05-29T07:00:37.267Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Bend, Oregon",
    "city": "Bend",
    "region": "OR",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.85
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T07:56:39.531Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Bend, Oregon",
      "city": "Bend",
      "region": "OR",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.85
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": "on_site",
  "salary_currency": null
}

{}

{
  "lists": [
    {
      "text": "Duties and Responsibilities ",
      "content": "<div><strong>Facility &amp; Process System Start-Up</strong></div>\n\n<li>Lead design and engineering activities associated with process equipment for new installations and/or continuous improvements</li>\n<li>Lead engineering activities for facility process systems through design, installation, and commissioning, including CIP, purified water, solvent distribution, and compressed gases</li>\n<li>Oversee process equipment installation, commissioning, and qualification (URS, FAT, SAT, IQ/OQ/PQ)</li>\n<li>Coordinate with vendors and contractors to ensure timely and compliant start-up of manufacturing systems</li>\n<li>Develop and execute commissioning plans, risk assessments, and readiness checklists</li>\n\n<div><strong>Process Design &amp; Optimization</strong></div>\n\n<li>Design and refine commercial-scale manufacturing processes for oral solid dosage forms and enabling technologies</li>\n<li>Perform capacity analysis, cycle time studies, and throughput modeling to ensure production efficiency</li>\n<li>Implement Lean and Six Sigma methodologies to reduce waste and improve process reliability</li>\n<li>Conduct formal risk assessments for existing process system to proactively mitigate quality and safety risks</li>\n\n<div><strong>Operational Readiness</strong></div>\n\n<li>Drive readiness activities for commercial launch, including supporting process validation and GMP documentation</li>\n<li>Partner with Validation, QA, and Manufacturing to ensure compliance with regulatory requirements</li>\n<li>Support tech transfer from development to commercial scale</li>\n<li>Collaborate with the Facilities and Maintenance teams to establish preventive and predictive maintenance schedules for process systems</li>\n<li>Draft and review standard operating procedures (SOPs) for the operation, cleaning, and troubleshooting of new process systems</li>\n\n<div><strong>Continuous Improvement</strong></div>\n\n<li>Analyze production data to identify bottlenecks and implement corrective actions</li>\n<li>Drive cost reduction initiatives and efficiency improvements without compromising quality</li>\n<li>Participate in deviation investigations and CAPA implementation</li>\n<li>Serve as the primary technical process system owner to ensure stable and robust manufacturing</li>\n\n<div><strong>Project Management</strong></div>\n\n<li>Contribute to project timelines, resource planning, and budget adherence</li>\n<li>Facilitate cross-functional project meetings and provide regular status updates to senior leadership</li>\n<li>Provide engineering input during client audits and regulatory inspections</li>\n<li>Proactively identify project risks and implement mitigation strategies&nbsp;</li>\n"
    },
    {
      "text": "Skills, Abilities and Education Requirements ",
      "content": "<div><strong>Required</strong></div>\n\n<li>BS/MS in Industrial Engineering, Chemical Engineering, Mechanical Engineering, or related discipline</li>\n<li>8+ years of experience in pharmaceutical manufacturing, process engineering, or industrial engineering</li>\n<li>Hands-on experience with facility start-up, commissioning, and equipment qualification</li>\n<li>Strong knowledge of cGMP requirements and commercial manufacturing operations</li>\n<li>Proficiency in process modeling, workflow analysis, and Lean/Six Sigma tools</li>\n<li>Excellent communication and documentation skills</li>\n\n<div>&nbsp;</div>\n<div><strong>Preferred</strong></div>\n\n<li>Experience with oral solid dosage forms and enabling technologies (e.g., spray drying, blending, granulation, tableting, encapsulation, &amp; tablet coating)</li>\n<li>Familiarity with facility design for regulated environments</li>\n<li>Knowledge of ERP/MES systems and digital manufacturing tools</li>\n<li>Project engineering experience in a regulated industry</li>\n\n<div>&nbsp;</div>\n<div><strong>Core Competencies</strong></div>\n\n<li>Analytical problem-solving and data-driven decision-making</li>\n<li>Ability to work cross-functionally in a fast-paced environment</li>\n<li>Strong organizational skills and attention to detail</li>\n<li>Continuous improvement mindset</li>\n"
    },
    {
      "text": "Physical Requirements ",
      "content": "\n<li>Prolonged periods of sitting or standing at a desk and working on a computer</li>\n<li>Prolonged periods of sitting, standing, and moving throughout a manufacturing environment</li>\n<li>Must be able to lift fifteen pounds at times</li>\n<li>Adheres to consistent and predictable in-person attendance</li>\n"
    }
  ],
  "country": "US",
  "createdAt": 1776716571627,
  "updatedAt": null,
  "categories": {
    "team": "Commercial Manufacturing",
    "location": "Bend, Oregon",
    "commitment": "Full-time Exempt",
    "department": "Product Commercialization",
    "allLocations": [
      "Bend, Oregon"
    ]
  },
  "salaryRange": null,
  "workplaceType": "onsite"
}