Quality Technician I

{
  "content_hash": "69e8688abdc988795d264290f62f15d675b548535f2592663976d52a34b8df71",
  "source_hash": "8c5e3c5e8ad6a55a8d0a2293c26be2d07fc8f899ef1b7e329c29099e1650f5c6",
  "last_changed_at": "2026-06-17T09:20:58.446Z",
  "active_status": "active"
}

{
  "dedupe": null,
  "language": "en",
  "location": {
    "raw": "Apex - Pittsfield - Pittsfield, MA 01201; 17 Downing Three, Building 1, Pittsfield, MA, 1201, USA",
    "city": "Pittsfield",
    "region": "MA",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": 35,
  "salary_min": 32,
  "inferred_at": "2026-06-22T10:05:07.790Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Apex - Pittsfield - Pittsfield, MA 01201; 17 Downing Three, Building 1, Pittsfield, MA, 1201, USA",
      "city": "Pittsfield",
      "region": "MA",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": "hour",
  "workplace_type": null,
  "salary_currency": "USD"
}

{}

{
  "detail": {
    "city": "Pittsfield",
    "jobId": 803516,
    "level": "",
    "endDate": "",
    "legalId": 50,
    "isHotJob": false,
    "jobShift": "",
    "jobTitle": "Quality Technician I",
    "location": "Apex - Pittsfield - Pittsfield, MA 01201",
    "startDate": "",
    "clientCode": "0VI76",
    "remoteType": "",
    "description": "<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>JOB SUMMARY: </b></span></span></p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">The Quality Technician is responsible for supporting the Quality Management System (QMS) in compliance with FDA regulations (21 CFR Part 820, and Part 11 as applicable) ISO 13485 and 9001 standards, and internal procedures. This role ensures timely execution of quality-related activities including documentation review, nonconformance processing, environmental monitoring, calibration tracking, and data integrity support.</span></span></p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">The Quality Technician plays a critical role in maintaining inspection readiness, supporting audits, and ensuring product quality and regulatory compliance.</span></span></p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Quality System Support</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Assist in maintaining compliance with industry regulations and standards, GMP requirements, and internal procedures</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support internal and external audit readiness activities</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Participate in internal audits and assist in audit response and closure</span></span></li>\r\n</ul>\r\n\r\n<p style=\"margin-left:48px\">&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Documentation &amp; Record Management</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Review and ensure completeness of quality records and production documentation</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support timely closure of records in accordance with ALCOA+ data integrity principles</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Maintain organized and inspection-ready documentation systems</span></span></li>\r\n</ul>\r\n\r\n<p style=\"margin-left:48px\">&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Nonconformance &amp; MRB Support</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Initiate, track, and assist in the investigation of Nonconformance Reports (NCRs)</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support Material Review Board (MRB) activities and documentation</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Ensure timely closure of quality events and proper documentation of dispositions</span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Calibration &amp; Equipment Control</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Track calibration schedules and maintain calibration records</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Coordinate calibration activities with internal teams and vendors</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Ensure equipment is compliant and within calibration requirements prior to use</span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Cleanroom &amp; Environmental Monitoring</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support routine monitoring of cleanroom conditions (e.g., particulate, temperature, humidity, pressure differentials)</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Review and trend environmental data for compliance</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support investigation and documentation of environmental excursions</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Ensure proper documentation and monitoring of controlled environments</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Assist in identifying and escalating environmental deviations</span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Change Control Support</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Assist in initiating and tracking change control requests</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Ensure required documentation and approvals are completed</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support implementation and closure of change controls</span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Supplier Quality Support</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Assist in maintaining supplier qualification records</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support incoming inspection and supplier performance monitoring</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Track supplier corrective actions and documentation</span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Software Validation &amp; Data Integrity</span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Support validation documentation for GxP software systems (e.g., IQ, OQ, PQ)</span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Perform routine audit trail reviews and support data integrity initiatives</span></span></li>\r\n</ul>\r\n",
    "jobCategory": "",
    "salaryRange": "$32.00 - $35.00 Hourly",
    "socialMedia": {
      "xLink": {
        "text": "Spectrum%2520Plastics%2520Group%2520Job%2520Opportunity%2520Quality%2520Technician%2520I"
      },
      "emailLink": {
        "subject": "Spectrum%20Plastics%20Group%20Job%20Opportunity%20Quality%20Technician%20I",
        "summary": "JOB%20SUMMARY%3A%20%0D%0A%0D%0AThe%20Quality%20Technician%20is%20responsible%20for%20supporting%20the%20Quality%20Management%20System%20%28QMS%29%20in%20compliance%20with%20FDA%20regulations%20%2821%20CFR%20Part%20820%2C%20and%20Part%2011%20as%20applicable%29%20ISO%2013485%20and%209001%20standards%2C%20and%20internal%20procedures.%20This%20role%20ensures%20timely%20execution%20of%20quality-related%20activities%20including%20documentation%20review%2C%20nonconformance%20processing%2C%20environmental%20monitoring%2C%20calibration%20tracking%2C%20and%20data%20integrity%20support.%0D%0A%0D%0AThe%20Quality%20Technician%20plays%20a%20critical%20role%20in%20maintaining%20inspection%20readiness%2C%20supporting%20audits%2C%20and%20ensuring%20product%20quality%20and%20regulatory%20compliance.%0D%0A%0D%0A%C2%0D%0A%0D%0AQuality%20System%20Support%0D%0A%0D%0A%0D%0A%09Assist%20in%20maintaining%20compliance%20with%20industry%20regulations%20and%20standards%2C%20GMP%20requirements%2C%20and%20internal%20procedures%0D%0A%09Support%20internal%20and%20external%20audit%20readiness%20activities%0D%0A%09Participate%20in%20internal%20audits%20and%20assist%20in%20audit%20response%20and%20closure%0D%0A%0D%0A%0D%0A%C2%0D%0A%0D%0ADocumentation%20%26%20Record%20Management%0D%0A%0D%0A%0D%0A%09Review%20and%20ensure%20completeness%20of%20quality%20records%20and%20production..."
      },
      "facebookLink": {
        "redirectUri": "",
        "facebookAppId": "773759036043100"
      },
      "linkedInLink": {}
    },
    "isQuickApply": false,
    "positionType": "Full Time",
    "countryPaidIn": "",
    "googleJobJson": "{\"@context\":\"https://schema.org/\",\"@type\":\"JobPosting\",\"title\":\"Quality Technician I\",\"identifier\":\"J0VI76803516\",\"url\":\"https://www.paycomonline.net/v4/ats/web.php/portal/F3CF2E6F06D96C7D42AC218710A77851/jobs/803516\",\"image\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=F3CF2E6F06D96C7D42AC218710A77851\",\"baseSalary\":{\"@type\":\"MonetaryAmount\",\"currency\":\"USD\",\"value\":{\"@type\":\"QuantitativeValue\",\"minValue\":32,\"maxValue\":35,\"unitText\":\"\"}},\"datePosted\":\"2026-06-16\",\"description\":\"Job DetailsJob Location: Apex - Pittsfield - Pittsfield, MA 01201Position Type: Full TimeSalary Range: $32.00 - $35.00 HourlyJOB SUMMARY: \\r\\n\\r\\nThe Quality Technician is responsible for supporting the Quality Management System (QMS) in compliance with FDA regulations (21 CFR Part 820, and Part 11 as applicable) ISO 13485 and 9001 standards, and internal procedures. This role ensures timely execution of quality-related activities including documentation review, nonconformance processing, environmental monitoring, calibration tracking, and data integrity support.\\r\\n\\r\\nThe Quality Technician plays a critical role in maintaining inspection readiness, supporting audits, and ensuring product quality and regulatory compliance.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nQuality System Support\\r\\n\\r\\n\\r\\n\\tAssist in maintaining compliance with industry regulations and standards, GMP requirements, and internal procedures\\r\\n\\tSupport internal and external audit readiness activities\\r\\n\\tParticipate in internal audits and assist in audit response and closure\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nDocumentation &amp; Record Management\\r\\n\\r\\n\\r\\n\\tReview and ensure completeness of quality records and production documentation\\r\\n\\tSupport timely closure of records in accordance with ALCOA+ data integrity principles\\r\\n\\tMaintain organized and inspection-ready documentation systems\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nNonconformance &amp; MRB Support\\r\\n\\r\\n\\r\\n\\tInitiate, track, and assist in the investigation of Nonconformance Reports (NCRs)\\r\\n\\tSupport Material Review Board (MRB) activities and documentation\\r\\n\\tEnsure timely closure of quality events and proper documentation of dispositions\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nCalibration &amp; Equipment Control\\r\\n\\r\\n\\r\\n\\tTrack calibration schedules and maintain calibration records\\r\\n\\tCoordinate calibration activities with internal teams and vendors\\r\\n\\tEnsure equipment is compliant and within calibration requirements prior to use\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nCleanroom &amp; Environmental Monitoring\\r\\n\\r\\n\\r\\n\\tSupport routine monitoring of cleanroom conditions (e.g., particulate, temperature, humidity, pressure differentials)\\r\\n\\tReview and trend environmental data for compliance\\r\\n\\tSupport investigation and documentation of environmental excursions\\r\\n\\tEnsure proper documentation and monitoring of controlled environments\\r\\n\\tAssist in identifying and escalating environmental deviations\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nChange Control Support\\r\\n\\r\\n\\r\\n\\tAssist in initiating and tracking change control requests\\r\\n\\tEnsure required documentation and approvals are completed\\r\\n\\tSupport implementation and closure of change controls\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSupplier Quality Support\\r\\n\\r\\n\\r\\n\\tAssist in maintaining supplier qualification records\\r\\n\\tSupport incoming inspection and supplier performance monitoring\\r\\n\\tTrack supplier corrective actions and documentation\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSoftware Validation &amp; Data Integrity\\r\\n\\r\\n\\r\\n\\tSupport validation documentation for GxP software systems (e.g., IQ, OQ, PQ)\\r\\n\\tPerform routine audit trail reviews and support data integrity initiatives\\r\\n\\r\\nQualificationsEDUCATION: \\r\\n\\r\\n\\r\\n\\tAssociate&rsquo;s or Bachelor&rsquo;s degree in a scientific, engineering, or related field preferred\\r\\n\\r\\n\\r\\nExperience\\r\\n\\r\\n\\r\\n\\t1&ndash;3 years of experience in a regulated industry (FDA, GMP, medical device, or pharmaceutical preferred)\\r\\n\\tExperience with Quality Systems and documentation practices\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSkills &amp; Competencies\\r\\n\\r\\n\\r\\n\\tKnowledge of FDA regulations (21 CFR Part 820, QSMR)\\r\\n\\tStrong attention to detail and organizational skills\\r\\n\\tAbility to manage multiple tasks and meet deadlines\\r\\n\\tFamiliarity with quality systems such as CAPA, NCR, and change control\\r\\n\\tProficiency in Microsoft Office and quality management software systems\\r\\n\\tStrong written and verbal communication skills\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWorking Conditions\\r\\n\\r\\n\\r\\n\\tInvolves work in cleanroom or controlled environments\\r\\n\\tUse of PPE as required\\r\\n\\tOccasional cross-functional collaboration with Operations, Engineering, and Quality teams\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nKey Performance Indicators (KPIs)\\r\\n\\r\\n\\r\\n\\tOn-time closure of quality records (NCRs, MRBs, change controls)\\r\\n\\tCalibration compliance rate\\r\\n\\tEnvironmental monitoring compliance\\r\\n\\tAudit readiness and documentation accuracy\\r\\n\\tReduction in backlog of quality system records\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWORKING CONDITIONS: \\r\\n\\r\\nWorks under general supervision while learning new concepts quickly. Requires light physical activity performing non-strenuous daily activities.&nbsp; \\r\\n\\r\\n\\r\\n\\tMust be able to lift up to 25 lbs.&nbsp; \\r\\n\\tMust be able to sit or stand for long periods of time \\r\\n\\tMust be able to climb up and down stairs\\r\\n\\tTravel is required to support company initiatives\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nNOTE: This job description is not intended to be an exhaustive list of all possible duties, responsibilities and/or qualifications. Other duties, responsibilities and/or qualifications may be assigned to this position.\\r\\n\",\"responsibilities\":\"JOB SUMMARY: \\r\\n\\r\\nThe Quality Technician is responsible for supporting the Quality Management System (QMS) in compliance with FDA regulations (21 CFR Part 820, and Part 11 as applicable) ISO 13485 and 9001 standards, and internal procedures. This role ensures timely execution of quality-related activities including documentation review, nonconformance processing, environmental monitoring, calibration tracking, and data integrity support.\\r\\n\\r\\nThe Quality Technician plays a critical role in maintaining inspection readiness, supporting audits, and ensuring product quality and regulatory compliance.\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nQuality System Support\\r\\n\\r\\n\\r\\n\\tAssist in maintaining compliance with industry regulations and standards, GMP requirements, and internal procedures\\r\\n\\tSupport internal and external audit readiness activities\\r\\n\\tParticipate in internal audits and assist in audit response and closure\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nDocumentation &amp; Record Management\\r\\n\\r\\n\\r\\n\\tReview and ensure completeness of quality records and production documentation\\r\\n\\tSupport timely closure of records in accordance with ALCOA+ data integrity principles\\r\\n\\tMaintain organized and inspection-ready documentation systems\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nNonconformance &amp; MRB Support\\r\\n\\r\\n\\r\\n\\tInitiate, track, and assist in the investigation of Nonconformance Reports (NCRs)\\r\\n\\tSupport Material Review Board (MRB) activities and documentation\\r\\n\\tEnsure timely closure of quality events and proper documentation of dispositions\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nCalibration &amp; Equipment Control\\r\\n\\r\\n\\r\\n\\tTrack calibration schedules and maintain calibration records\\r\\n\\tCoordinate calibration activities with internal teams and vendors\\r\\n\\tEnsure equipment is compliant and within calibration requirements prior to use\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nCleanroom &amp; Environmental Monitoring\\r\\n\\r\\n\\r\\n\\tSupport routine monitoring of cleanroom conditions (e.g., particulate, temperature, humidity, pressure differentials)\\r\\n\\tReview and trend environmental data for compliance\\r\\n\\tSupport investigation and documentation of environmental excursions\\r\\n\\tEnsure proper documentation and monitoring of controlled environments\\r\\n\\tAssist in identifying and escalating environmental deviations\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nChange Control Support\\r\\n\\r\\n\\r\\n\\tAssist in initiating and tracking change control requests\\r\\n\\tEnsure required documentation and approvals are completed\\r\\n\\tSupport implementation and closure of change controls\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSupplier Quality Support\\r\\n\\r\\n\\r\\n\\tAssist in maintaining supplier qualification records\\r\\n\\tSupport incoming inspection and supplier performance monitoring\\r\\n\\tTrack supplier corrective actions and documentation\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSoftware Validation &amp; Data Integrity\\r\\n\\r\\n\\r\\n\\tSupport validation documentation for GxP software systems (e.g., IQ, OQ, PQ)\\r\\n\\tPerform routine audit trail reviews and support data integrity initiatives\\r\\n\\r\\n\",\"employmentType\":\"FULL_TIME\",\"hiringOrganization\":{\"@type\":\"Organization\",\"name\":\"Spectrum Plastics Group\",\"logo\":\"https://www.paycomonline.net/v4/ats/web.php/application/style/logo?clientkey=F3CF2E6F06D96C7D42AC218710A77851\"},\"jobLocation\":{\"@type\":\"Place\",\"address\":{\"streetAddress\":\"17 Downing Three, Building 1\",\"addressLocality\":\"Pittsfield\",\"addressRegion\":\"MA\",\"postalCode\":1201,\"addressCountry\":\"USA\"}},\"qualifications\":\"EDUCATION: \\r\\n\\r\\n\\r\\n\\tAssociate&rsquo;s or Bachelor&rsquo;s degree in a scientific, engineering, or related field preferred\\r\\n\\r\\n\\r\\nExperience\\r\\n\\r\\n\\r\\n\\t1&ndash;3 years of experience in a regulated industry (FDA, GMP, medical device, or pharmaceutical preferred)\\r\\n\\tExperience with Quality Systems and documentation practices\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSkills &amp; Competencies\\r\\n\\r\\n\\r\\n\\tKnowledge of FDA regulations (21 CFR Part 820, QSMR)\\r\\n\\tStrong attention to detail and organizational skills\\r\\n\\tAbility to manage multiple tasks and meet deadlines\\r\\n\\tFamiliarity with quality systems such as CAPA, NCR, and change control\\r\\n\\tProficiency in Microsoft Office and quality management software systems\\r\\n\\tStrong written and verbal communication skills\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWorking Conditions\\r\\n\\r\\n\\r\\n\\tInvolves work in cleanroom or controlled environments\\r\\n\\tUse of PPE as required\\r\\n\\tOccasional cross-functional collaboration with Operations, Engineering, and Quality teams\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nKey Performance Indicators (KPIs)\\r\\n\\r\\n\\r\\n\\tOn-time closure of quality records (NCRs, MRBs, change controls)\\r\\n\\tCalibration compliance rate\\r\\n\\tEnvironmental monitoring compliance\\r\\n\\tAudit readiness and documentation accuracy\\r\\n\\tReduction in backlog of quality system records\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWORKING CONDITIONS: \\r\\n\\r\\nWorks under general supervision while learning new concepts quickly. Requires light physical activity performing non-strenuous daily activities.&nbsp; \\r\\n\\r\\n\\r\\n\\tMust be able to lift up to 25 lbs.&nbsp; \\r\\n\\tMust be able to sit or stand for long periods of time \\r\\n\\tMust be able to climb up and down stairs\\r\\n\\tTravel is required to support company initiatives\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nNOTE: This job description is not intended to be an exhaustive list of all possible duties, responsibilities and/or qualifications. Other duties, responsibilities and/or qualifications may be assigned to this position.\\r\\n\",\"experienceRequirements\":\"EDUCATION: \\r\\n\\r\\n\\r\\n\\tAssociate&rsquo;s or Bachelor&rsquo;s degree in a scientific, engineering, or related field preferred\\r\\n\\r\\n\\r\\nExperience\\r\\n\\r\\n\\r\\n\\t1&ndash;3 years of experience in a regulated industry (FDA, GMP, medical device, or pharmaceutical preferred)\\r\\n\\tExperience with Quality Systems and documentation practices\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nSkills &amp; Competencies\\r\\n\\r\\n\\r\\n\\tKnowledge of FDA regulations (21 CFR Part 820, QSMR)\\r\\n\\tStrong attention to detail and organizational skills\\r\\n\\tAbility to manage multiple tasks and meet deadlines\\r\\n\\tFamiliarity with quality systems such as CAPA, NCR, and change control\\r\\n\\tProficiency in Microsoft Office and quality management software systems\\r\\n\\tStrong written and verbal communication skills\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWorking Conditions\\r\\n\\r\\n\\r\\n\\tInvolves work in cleanroom or controlled environments\\r\\n\\tUse of PPE as required\\r\\n\\tOccasional cross-functional collaboration with Operations, Engineering, and Quality teams\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nKey Performance Indicators (KPIs)\\r\\n\\r\\n\\r\\n\\tOn-time closure of quality records (NCRs, MRBs, change controls)\\r\\n\\tCalibration compliance rate\\r\\n\\tEnvironmental monitoring compliance\\r\\n\\tAudit readiness and documentation accuracy\\r\\n\\tReduction in backlog of quality system records\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nWORKING CONDITIONS: \\r\\n\\r\\nWorks under general supervision while learning new concepts quickly. Requires light physical activity performing non-strenuous daily activities.&nbsp; \\r\\n\\r\\n\\r\\n\\tMust be able to lift up to 25 lbs.&nbsp; \\r\\n\\tMust be able to sit or stand for long periods of time \\r\\n\\tMust be able to climb up and down stairs\\r\\n\\tTravel is required to support company initiatives\\r\\n\\r\\n\\r\\n&nbsp;\\r\\n\\r\\n&nbsp;\\r\\n\\r\\nNOTE: This job description is not intended to be an exhaustive list of all possible duties, responsibilities and/or qualifications. Other duties, responsibilities and/or qualifications may be assigned to this position.\\r\\n\",\"validThrough\":\"2026-08-31\"}",
    "applyAvailable": true,
    "educationLevel": "",
    "qualifications": "<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>EDUCATION: </b></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Associate&rsquo;s or Bachelor&rsquo;s degree in a scientific, engineering, or related field preferred</span></span></span></li>\r\n</ul>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>Experience</b></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">1&ndash;3 years of experience in a regulated industry (FDA, GMP, medical device, or pharmaceutical preferred)</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Experience with Quality Systems and documentation practices</span></span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>Skills &amp; Competencies</b></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Knowledge of FDA regulations (21 CFR Part 820, QSMR)</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Strong attention to detail and organizational skills</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Ability to manage multiple tasks and meet deadlines</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Familiarity with quality systems such as CAPA, NCR, and change control</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Proficiency in Microsoft Office and quality management software systems</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Strong written and verbal communication skills</span></span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>Working Conditions</b></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Involves work in cleanroom or controlled environments</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Use of PPE as required</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Occasional cross-functional collaboration with Operations, Engineering, and Quality teams</span></span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>Key Performance Indicators (KPIs)</b></span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">On-time closure of quality records (NCRs, MRBs, change controls)</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Calibration compliance rate</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Environmental monitoring compliance</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Audit readiness and documentation accuracy</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Reduction in backlog of quality system records</span></span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>WORKING CONDITIONS:</b> </span></span></p>\r\n\r\n<p><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Works under general supervision while learning new concepts quickly. Requires light physical activity performing non-strenuous daily activities.&nbsp; </span></span></p>\r\n\r\n<ul>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Must be able to lift up to 25 lbs.&nbsp; </span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Must be able to sit or stand for long periods of time </span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Must be able to climb up and down stairs</span></span></span></li>\r\n\t<li><span style=\"font-size:12pt\"><span style=\"tab-stops:list .5in\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\">Travel is required to support company initiatives</span></span></span></li>\r\n</ul>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p>&nbsp;</p>\r\n\r\n<p align=\"center\" style=\"text-align:center\"><span style=\"font-size:12pt\"><span style=\"font-family:&quot;Times New Roman&quot;,serif\"><b>NOTE: This job description is not intended to be an exhaustive list of all possible duties, responsibilities and/or qualifications. Other duties, responsibilities and/or qualifications may be assigned to this position.</b></span></span></p>\r\n",
    "descriptionTitle": "Description",
    "travelPercentage": "",
    "jobYoutubeVideoId": "",
    "legalRevisionDate": {
      "date": "2024-09-03T16:19:19.000Z",
      "timezone": "America/Chicago",
      "timezone_type": 3
    },
    "secondaryLocations": [],
    "primaryPhoneCountry": "US",
    "primaryPhoneEnabled": true,
    "qualificationsTitle": "Qualifications",
    "primaryPhoneRequired": true,
    "primaryPhoneNumberDoesNotExist": false
  },
  "preview": {
    "jobId": 803516,
    "isHotJob": false,
    "jobTitle": "Quality Technician I",
    "postedOn": "",
    "locations": "Apex - Pittsfield - Pittsfield, MA 01201",
    "remoteType": "",
    "description": "JOB SUMMARY: \r\n\r\nThe Quality Technician is responsible for supporting the Quality Management System (QMS) in compliance with FDA regulations (21 CFR P...",
    "positionType": "Full Time"
  },
  "detail_meta": {
    "url": "https://portal-applicant-tracking.us-cent.paycomonline.net/api/ats/job-postings/803516",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 38370
  },
  "detail_errors": []
}