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Quality Engineer

240d4421 5b39 45d4 A140 4a3e00eab57f 19000101 000001 · West Warwick, RI, US, West Warwick, RI · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
Company240d4421 5b39 45d4 A140 4a3e00eab57f 19000101 000001
TitleQuality Engineer
Normalized title-
Department / team-
LocationWest Warwick, RI, United States
Work model-
Employment type-
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-03-04 / 2026-05-31
Changed / last seen2026-06-22 / 2026-06-22

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PageWhat it containsOpen
Company jobsActive postings from 240d4421 5b39 45d4 A140 4a3e00eab57f 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in West Warwick.Open
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Linked records

Company240d4421 5b39 45d4 A140 4a3e00eab57f 19000101 000001
Source184105ff-2dc6-465c-8409-f46228c9c46e
ATS providerADP Workforce Now Recruiting

Description

Job Title: Quality Engineer Reports to: Quality Operations Manager Job Function: The Quality Engineer supports quality systems and product quality for a personal care contract manufacturing operation. This role has no direct reports and works cross‑functionally with Operations, Engineering, R&D, and Customer Service to ensure compliance with customer, regulatory (ISO, FDA, Organic, etc.), and internal requirements. The Quality Engineer plays a key role in audits, root cause analysis, and customer complaint management while driving continuous improvement across the site. Essential Duties and Responsibilities: Quality Systems and Compliance Support and maintain site quality systems in compliance with regulatory (ISO, GMP, FDA, etc.) and applicable customer requirements. Lead internal audits, customer audits, and third‑party audits; prepare documentation, support on‑site activities, and ensure timely closure of audit findings. Assist with document control, SOP updates, and change management activities. Support risk assessments, control plans, and quality metrics reporting. Root Cause Analysis & Corrective Actions Lead and facilitate root cause analysis using structured problem‑solving tools (e.g., 5 Whys, Fishbone, FMEA). Develop, implement, and track corrective and preventive actions (CAPAs) to ensure effectiveness and sustainability. Partner with Operations and Engineering to address quality issues, reduce defects, and improve process capability Customer Complaint Management Manage customer complaints from receipt through closure, including investigation, root cause analysis, corrective action development and implementation, and response preparation. Coordinate cross‑functional investigations to ensure timely, accurate, and professional customer responses. Identify complaint trends and drive systemic improvements to prevent recurrence. Manufacturing & Process Support Provide quality support to manufacturing operations, including deviation investigations and nonconformance management. Support sampling, documentation, and shipment of raw materials, batch, and finished product samples to outside labs for testing. Support new product introductions (NPI), validation protocols (IQ/OQ/PQ), and process changes and subsequent process change control from a quality perspective. Review batch records, inspection data, and quality documentation as needed. Continuous Improvement Analyze quality data to identify trends, risks, and improvement opportunities. Participate in Lean, Six Sigma, or other continuous improvement initiatives. Promote a culture of quality, compliance, and accountability throughout the organization. Minimum Knowledge, Skills and Abilities: Bachelor’s degree in Engineering, Quality, Chemistry, or a related technical field. 3+ years of quality engineering or quality assurance experience in a manufacturing environment. Experience with audits, nonconformance investigations, customer complaint management, root cause analysis, CAPA development and implementation. Working knowledge of GMP and quality management systems. Strong analytical, organizational, and problem‑solving skills. Effective written and verbal communication skills. Preference for Lean, Six Sigma or quality certification. Familiarity with regulatory compliance requirements applicable to certifications such as organic, Halal, naturals etc… would be desirable. Physical & Work Environment: Manufacturing environment with regular presence on the production floor. Ability to sit, stand, walk, and occasionally lift up to 25 lbs. Occasional travel for customer or supplier audits may be required.

Full job record

Job ID0462a0a39f6113acc57a4f235d2258624f27731e
Org ID10a75bdb-3159-447f-b9ab-bed0884a5983
Source ID184105ff-2dc6-465c-8409-f46228c9c46e
Board ID184105ff-2dc6-465c-8409-f46228c9c46e
Provideradp_workforcenow
Provider Job Key573043
TitleQuality Engineer
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Statusactive
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Location TextWest Warwick, RI, US, West Warwick, RI
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CountryUnited States
RegionRI
CityWest Warwick
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Source URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=240d4421-5b39-45d4-a140-4a3e00eab57f&ccId=19000101_000001&lang=en_US&type=JS&jobId=573043&jwId=9201936296798_1
Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=240d4421-5b39-45d4-a140-4a3e00eab57f&ccId=19000101_000001&lang=en_US&type=JS&jobId=573043&jwId=9201936296798_1
First Seen At2026-05-31 18:22:24Z
Last Seen At2026-06-22 12:18:39Z
Last Checked At2026-06-22 12:18:39Z
Last Changed At2026-06-22 12:18:39Z
Inactive At—
Source Posted At2026-03-04 00:14:00Z
Source Updated At—
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=240d4421-5b39-45d4-a140-4a3e00eab57f|19000101_000001/date=2026-06-22/2026-06-22T12-18-38-650Z-239b6deb27dec2db76253bdb0777c0607702254ce61273d8812b05b1341c6586.json
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    "requisitionDescription": "<div><h1 style='margin:0in;text-align:center;font-size:19px;font-family:\"Times New Roman\",serif;font-weight:normal;' data-pasted=\"true\"><strong><span style=\"font-size:15px;\">&nbsp;</span></strong></h1><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;text-align:center;'><strong><span style='font-family:\"Aptos\",sans-serif;'>&nbsp;</span></strong></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;'>Job Title: </span></strong><span style='font-family:\"Aptos\",sans-serif;'>Quality Engineer&nbsp;</span></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;'><span style='font-family:\"Aptos\",sans-serif;'><strong>Reports to:&nbsp;</strong>Quality Operations Manager</span></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;border:none;padding:0in;'><span style='font-family:\"Aptos\",sans-serif;'>&nbsp;</span></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;'><span style='font-family:\"Aptos\",sans-serif;'>&nbsp;</span></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>Job Function:</span></strong></p><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;color:black;border:none;border-bottom:solid windowtext 1.5pt;padding:0in 0in 1.0pt 0in;'><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;border:none;padding:0in;'><span style='font-family:\"Aptos\",sans-serif;'>The Quality Engineer supports quality systems and product quality for a personal care contract manufacturing operation. This role has no direct reports and works cross‑functionally with Operations, Engineering, R&amp;D, and Customer Service to ensure compliance with customer, regulatory (ISO, FDA, Organic, etc.), and internal requirements. The Quality Engineer plays a key role in audits, root cause analysis, and customer complaint management while driving continuous improvement across the site.</span></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;border:none;padding:0in;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>&nbsp;</span></strong></p></div><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>Essential Duties and Responsibilities:</span></strong></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>Quality Systems and Compliance</span></strong></p><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;color:black;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0in;\"><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Support and maintain site quality systems in compliance with regulatory (ISO, GMP, FDA, etc.) and applicable customer requirements.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Lead internal audits, customer audits, and third‑party audits; prepare documentation, support on‑site activities, and ensure timely closure of audit findings.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Assist with document control, SOP updates, and change management activities.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Support risk assessments, control plans, and quality metrics reporting.</span></li></ul></div><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;'><span style='font-size:15px;font-family:\"Aptos\",sans-serif;'>&nbsp;</span></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;'><strong><span style='font-size:15px;font-family:\"Aptos\",sans-serif;'>Root Cause Analysis &amp; Corrective Actions</span></strong></p><ul type=\"disc\" style=\"margin-bottom:0in;\"><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Lead and facilitate root cause analysis using structured problem‑solving tools (e.g., 5 Whys, Fishbone, FMEA).</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Develop, implement, and track corrective and preventive actions (CAPAs) to ensure effectiveness and sustainability.</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Partner with Operations and Engineering to address quality issues, reduce defects, and improve process capability</span></li></ul><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>Customer Complaint Management</span></strong></p><ul type=\"disc\" style=\"margin-bottom:0in;\"><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Manage customer complaints from receipt through closure, including investigation, root cause analysis, corrective action development and implementation, and response preparation.</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Coordinate cross‑functional investigations to ensure timely, accurate, and professional customer responses.</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Identify complaint trends and drive systemic improvements to prevent recurrence.</span></li></ul><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>Manufacturing &amp; Process Support</span></strong></p><ul type=\"disc\" style=\"margin-bottom:0in;\"><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Provide quality support to manufacturing operations, including deviation investigations and nonconformance management.</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Support sampling, documentation, and shipment of raw materials, batch, and finished product samples to outside labs for testing.&nbsp;</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Support new product introductions (NPI), validation protocols (IQ/OQ/PQ), and process changes and subsequent process change control from a quality perspective.</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Review batch records, inspection data, and quality documentation as needed.</span></li></ul><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>Continuous Improvement</span></strong></p><ul type=\"disc\" style=\"margin-bottom:0in;\"><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Analyze quality data to identify trends, risks, and improvement opportunities.</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Participate in Lean, Six Sigma, or other continuous improvement initiatives.</span></li><li style=\"margin:0in;line-height:normal;font-size:15px;font-family: initial;color:windowtext;\"><span style='font-family:     \"Aptos\",sans-serif;'>Promote a culture of quality, compliance, and accountability throughout the organization.</span></li></ul><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>&nbsp;</span></strong></p><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:normal;color:black;'><strong><span style='font-family:\"Aptos\",sans-serif;color:windowtext;'>Minimum Knowledge, Skills and Abilities:</span></strong></p><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;color:black;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0in;\"><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Bachelor&rsquo;s degree in Engineering, Quality, Chemistry, or a related technical field.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>3+ years of quality engineering or quality assurance experience in a manufacturing environment.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Experience with audits, nonconformance investigations, customer complaint management, root cause analysis, CAPA development and implementation.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Working knowledge of GMP and quality management systems.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Strong analytical, organizational, and problem‑solving skills.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Effective written and verbal communication skills.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Preference for Lean, Six Sigma or quality certification.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Familiarity with regulatory compliance requirements applicable to certifications such as organic, Halal, naturals etc&hellip; would be desirable.</span></li></ul></div><p style='margin-right:0in;margin-left:0in;font-size:15px;font-family:\"Arial\",sans-serif;margin:0in;line-height:115%;color:black;'><strong><span style='font-size:15px;font-family:\"Aptos\",sans-serif;'>Physical &amp; Work Environment:</span></strong></p><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;color:black;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0in;\"><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Manufacturing environment with regular presence on the production floor.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Ability to sit, stand, walk, and occasionally lift up to 25 lbs.</span></li><li style=\"margin:0in;line-height:115%;font-size:15px;font-family: initial;color:black;\"><span style='font-family:\"Aptos\",sans-serif;font-size:15px;'>Occasional travel for customer or supplier audits may be required.</span></li></ul></div></div>\n",
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    },
    "requisitionTitle": "Quality Engineer",
    "clientRequisitionID": "1088",
    "organizationalUnits": [],
    "postingInstructions": [],
    "additionalProperties": {},
    "requisitionLocations": [
      {
        "address": {
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        },
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    "screeningRequirements": [],
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  "detail_meta": {
    "url": "https://workforcenow.adp.com/mascsr/default/careercenter/public/events/staffing/v1/job-requisitions/573043?cid=240d4421-5b39-45d4-a140-4a3e00eab57f&ccId=19000101_000001&lang=en_US&locale=en_US",
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}
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Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/0462a0a39f6113acc57a4f235d2258624f27731e?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/10a75bdb-3159-447f-b9ab-bed0884a5983JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/184105ff-2dc6-465c-8409-f46228c9c46eJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/0462a0a39f6113acc57a4f235d2258624f27731e/eventsJSON

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