QUALITY ENGINEER

{
  "content_hash": "6d4f78f01a0056ede5d9cd5f441f9c4cb5afeaeaa26d5888e6b4d4cf34bb7304",
  "source_hash": "2a6f914ca2cb310642f109e58fa8c81a0551c1681ed6ff02adf84f814a3c46fa",
  "last_changed_at": "2026-05-30T06:12:20.343Z",
  "active_status": "active"
}

{
  "dedupe": null,
  "language": "en",
  "location": {
    "raw": "Nephron SC, LLC",
    "city": "West Columbia",
    "region": "SC",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-21T14:28:03.410Z",
  "launch_scope": {
    "reason": "paylocity_production_catalog",
    "included": true,
    "location": {
      "raw": "Nephron SC, LLC",
      "city": "West Columbia",
      "region": "SC",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}

{}

{
  "detail": {
    "url": "https://recruiting.paylocity.com/recruiting/jobs/Details/4067218/Nephron-Pharmaceuticals/QUALITY-ENGINEER",
    "job_type": null,
    "pageData": {
      "jobTitle": "QUALITY ENGINEER",
      "moduleName": "Nephron Pharmaceuticals",
      "showSocialWidget": true
    },
    "apply_path": "/Recruiting/jobs/Apply/4067218",
    "html_title": "Nephron Pharmaceuticals - QUALITY ENGINEER",
    "description_html": "<p>&nbsp;&nbsp;</p><p><strong>Job Purpose:&nbsp;</strong></p><p>The Quality Engineer supports aseptic manufacturing operations by executing quality system activities, participating in facility and equipment commissioning, and driving process improvements. This role works cross-functionally with Manufacturing, Engineering, MS&amp;T, and Quality to ensure compliance with cGMP requirements while supporting both development and commercial manufacturing programs.</p><p>This position includes hands-on involvement in cleanroom environments and requires strong technical, analytical, and documentation skills.</p><p><br></p><p><strong>Essential Duties and Responsibilities:</strong></p><p>· Execute and support cGMP operations and project-based work, including commissioning activities, process studies, and quality system initiatives&nbsp;</p><p>· Participate directly in facility and equipment commissioning activities, including field execution, documentation, and coordination with engineering and operations teams&nbsp;</p><p>· Support and execute process and product development studies, including data collection, analysis, and documentation&nbsp;</p><p>· Contribute to technology transfer and scale-up activities, supporting successful transition from development to manufacturing&nbsp;</p><p>· Participate in cleanroom and controlled environment activities, including:&nbsp;</p><p>· Supporting airflow visualization (smoke studies)&nbsp;</p><p>· Assisting with cleanroom setup, readiness, and operational support&nbsp;</p><p>· Execute and support CAPA-related projects, including root cause analysis, implementation of corrective and preventive actions, and effectiveness checks&nbsp;</p><p>· Support deviations, investigations, and change controls through data gathering, documentation, and implementation of actions&nbsp;</p><p>· Ensure all work is documented in accordance with cGMP requirements, maintaining accuracy, completeness, and data integrity&nbsp;</p><p>· Collaborate cross-functionally with Manufacturing, Engineering, MS&amp;T, and Quality teams to support facility startup, operational readiness, and continuous improvement initiatives&nbsp;</p><p>· Participate in risk assessments and support mitigation activities related to processes, equipment, and cleanroom environments&nbsp;</p><p>· Contribute to inspection readiness efforts, including documentation support and response to audit observations&nbsp;</p><p>· Identify and support process and operational improvements across development and manufacturing activities&nbsp;</p>",
    "jsonld_jobposting": {
      "@type": "JobPosting",
      "title": "QUALITY ENGINEER",
      "@context": "https://schema.org",
      "datePosted": "2026-04-13T20:32:50-05:00",
      "description": "<p>Description</p><p>  </p><p><strong>Job Purpose: </strong></p><p>The Quality Engineer supports aseptic manufacturing operations by executing quality system activities, participating in facility and equipment commissioning, and driving process improvements. This role works cross-functionally with Manufacturing, Engineering, MS&T, and Quality to ensure compliance with cGMP requirements while supporting both development and commercial manufacturing programs.</p><p>This position includes hands-on involvement in cleanroom environments and requires strong technical, analytical, and documentation skills.</p><p><br/></p><p><strong>Essential Duties and Responsibilities:</strong></p><p>· Execute and support cGMP operations and project-based work, including commissioning activities, process studies, and quality system initiatives </p><p>· Participate directly in facility and equipment commissioning activities, including field execution, documentation, and coordination with engineering and operations teams </p><p>· Support and execute process and product development studies, including data collection, analysis, and documentation </p><p>· Contribute to technology transfer and scale-up activities, supporting successful transition from development to manufacturing </p><p>· Participate in cleanroom and controlled environment activities, including: </p><p>· Supporting airflow visualization (smoke studies) </p><p>· Assisting with cleanroom setup, readiness, and operational support </p><p>· Execute and support CAPA-related projects, including root cause analysis, implementation of corrective and preventive actions, and effectiveness checks </p><p>· Support deviations, investigations, and change controls through data gathering, documentation, and implementation of actions </p><p>· Ensure all work is documented in accordance with cGMP requirements, maintaining accuracy, completeness, and data integrity </p><p>· Collaborate cross-functionally with Manufacturing, Engineering, MS&T, and Quality teams to support facility startup, operational readiness, and continuous improvement initiatives </p><p>· Participate in risk assessments and support mitigation activities related to processes, equipment, and cleanroom environments </p><p>· Contribute to inspection readiness efforts, including documentation support and response to audit observations </p><p>· Identify and support process and operational improvements across development and manufacturing activities </p><p>Requirements</p><p>  </p><p><strong>Education / Experience: </strong></p><p>· Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a related field.</p><p>· 2-5 years of experience in pharmaceutical manufacturing or a related industry, with a strong understanding of pharmaceutical processes and GMP.</p><p>· Experience with commissioning/startup activities, cleanroom and contamination control practices (including smoke studies), process automation systems, validation, and cGMP/FDA regulatory requirements preferred.</p><p><br/></p><p><strong>Working Conditions / Physical Requirements:</strong></p><p>· Position requires bending (desk to floor), lifting (up to 15 lbs.), corrected vision (20/20), standing, sitting, typing, and walking.</p><p>· Ability to work in cleanroom environments, including gowning requirements.</p>",
      "jobLocation": {
        "@type": "Place",
        "address": {
          "@type": "PostalAddress",
          "postalCode": "29172",
          "addressRegion": "SC",
          "streetAddress": "4500 12th Street Extension",
          "addressCountry": "US",
          "addressLocality": "West Columbia"
        }
      },
      "hiringOrganization": {
        "logo": "https://recruiting.paylocity.com/recruiting/jobs/GetLogoFile?moduleId=9003",
        "name": "NEPHRON SC, LLC",
        "@type": "Organization"
      }
    },
    "requirements_html": "<p>&nbsp;&nbsp;</p><p><strong>Education / Experience:&nbsp;</strong></p><p>· Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a related field.</p><p>· 2-5 years of experience in pharmaceutical manufacturing or a related industry, with a strong understanding of pharmaceutical processes and GMP.</p><p>· Experience with commissioning/startup activities, cleanroom and contamination control practices (including smoke studies), process automation systems, validation, and cGMP/FDA regulatory requirements preferred.</p><p><br></p><p><strong>Working Conditions / Physical Requirements:</strong></p><p>· Position requires bending (desk to floor), lifting (up to 15 lbs.), corrected vision (20/20), standing, sitting, typing, and walking.</p><p>· Ability to work in cleanroom environments, including gowning requirements.</p>",
    "requirements_text": "Education / Experience:\n · Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Industrial Engineering, or a related field.\n · 2-5 years of experience in pharmaceutical manufacturing or a related industry, with a strong understanding of pharmaceutical processes and GMP.\n · Experience with commissioning/startup activities, cleanroom and contamination control practices (including smoke studies), process automation systems, validation, and cGMP/FDA regulatory requirements preferred.\n Working Conditions / Physical Requirements:\n · Position requires bending (desk to floor), lifting (up to 15 lbs.), corrected vision (20/20), standing, sitting, typing, and walking.\n · Ability to work in cleanroom environments, including gowning requirements."
  },
  "list_job": {
    "JobId": 4067218,
    "IsRemote": false,
    "JobTitle": "QUALITY ENGINEER",
    "IsInternal": false,
    "Description": "",
    "JobLocation": {
      "Zip": "29172",
      "City": "West Columbia",
      "Name": "Nephron SC, LLC",
      "Metro": null,
      "State": "SC",
      "County": null,
      "Address": "4500 12th Street Extension",
      "Country": "USA",
      "Address2": null,
      "ModuleId": 9003,
      "LocationId": 3992241,
      "SmartyAddressId": "00000000-0000-0000-0000-000000000000"
    },
    "LocationName": "Nephron SC, LLC",
    "PublishedDate": "2026-04-07T15:09:22-05:00",
    "HiringDepartment": null,
    "IndeedRemoteType": 2,
    "ShouldDisplayLocation": true
  },
  "detail_errors": []
}