bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesHccg Fa Us2 Oraclecloud Com CXQuality Manager

Quality Manager

Hccg Fa Us2 Oraclecloud Com CX · Freeport, TX, United States; Freeport, Freeport, TX, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyHccg Fa Us2 Oraclecloud Com CX
TitleQuality Manager
Normalized title-
Department / team-
LocationFreeport, TX, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-03-30 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Hccg Fa Us2 Oraclecloud Com CX.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Oracle Recruiting Cloud / Fusion HCM.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Freeport.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyHccg Fa Us2 Oraclecloud Com CX
Source75bb0d91-4a48-4a97-b769-106bf2f05b05
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description The Role: The Quality Manager will ensure that the site meets GMP, compliance and regulatory standards. You will maintain the site in compliance with IS0 9001 standard are manufactured under GMP regulations and all shipped pharma products are of good quality. How You Will Make an Impact: Ensure EHS compliance and continuous improvement in EHS performance Ensure department goals and KPIs are aligned with site objectives Develop budget plans following a zero-based approach and manage Quality costs Provide site strategy for quality management Be the Management Representative for obtaining and maintaining quality certifications (ISO 9001 etc.) Oversee execution of raw material and finished good testing and COA generation Provide site strategy and procedures for maintenance of analytical data and document control Provide strategy for in-process quality control Oversee laboratory, analytical equipment and facilities Review customer specifications and ensure that processes are capable Analyze and lead improvement efforts related to process capabilities (CpK) of production processes to eliminate product defects Focal point for site customer complaint investigation and response processes Ensure EHS compliance and continuous improvement in EHS performance Assure a compliant quality operation (incl. e.g. Responsible Care, ISO 9001/14001) Manage QA aspects of the site MOC process for pharma and non-pharma operations. Create and improve customer engagement touchpoints for matters related to product quality and regulatory compliance Assess and evaluate supplier quality processes to ensure alignment with SI quality standards; apply corrective action accordingly Oversee audit and investigation processes related to quality and for corrective measures to achieve and maintain compliance Evaluate and improve quality process work plans to reduce product rejection rates Assure the operation, maintaining, and improvements of the site's GMP and MOC processes Maintain FDA export certifications for regulatory bodies world-wide (US, Canada, EU, Mexico, Brazil, Japan) when applicable Active participation in any regional QA associated initiatives (internal/external) Serve as member of Site Leadership Team Work with other functional leaders to identify and solve problems to support achievement of site goals Anticipate future requirements for site and develop strategic plans to meet them Creating Extraordinary Starts With: Bachelor's degree in Chemistry or Chemical Engineering, or other STEM discipline Minimum of ten years' experience in process industry manufacturing Minimum of five years Supervisory experience Deep level of chemistry knowledge with training in analytical chemistry and experience in raw material and finished good testing, in-process quality control, Quality Certification Management, quality auditing quality statistics ISO 9001, 1400, RC1400 knowledge certification; ISO Auditor; cGMP certifications preferred What We Value: We strive for all employees to nurture physical, mental and emotional health both personally and professionally. Our commitment to health and wellness centers around prevention, early detection and embracing a healthy lifestyle. Some offerings may vary by role or region, but may include: Physical Health benefits including competitive Medical, Dental, and Vision packages, company contribution to Health Savings Account, cash incentive for Annual Physical and reimbursement Financial Wellness opportunities including company paid life insurance and disability plans, 401(k) Retirement Plan with generous company match, and certified Financial Planning & Investment services Mental Health benefits including generous Paid Time Off and 10 Paid Holidays, Paid Parental Bonding Leave, and much more! Company Essential Solutions with Extraordinary Results SI Group is a global leader in the innovative technology of performance additives, process solutions, active pharmaceutical ingredients, and chemical intermediates. Our solutions are essential to many diverse industries and applications, creating extraordinary results. We drive value by enhancing the quality, performance, and durability of countless items we use every day. We are on a journey to captivate our customers at every level. Whether that means expanding our capabilities, global reach, or providing new innovations and technologies that create value. Our approach is customized to exceed customer needs and deliver superior performance.

Full job record

Job IDc3c063494c0d6948c668cc4dffd61ac3f64dd645
Org IDe5efa4f0-3d01-4911-bb0e-446eda2c8723
Source ID75bb0d91-4a48-4a97-b769-106bf2f05b05
Board ID75bb0d91-4a48-4a97-b769-106bf2f05b05
Provideroracle_hcm
Provider Job Key1430
TitleQuality Manager
Normalized Title
Statusactive
Activeyes
Location TextFreeport, TX, United States; Freeport, Freeport, TX, US
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionTX
CityFreeport
Salary RawDescription The Role: The Quality Manager will ensure that the site meets GMP, compliance and regulatory standards. You will maintain the site in compliance with IS0 9001 standard are manufactured under GMP regulations and all shipped pharma products are of good quality. How You Will Make an Impact: Ensure EHS compliance and continuous improvement in EHS performance Ensure department goals and KPIs are aligned with site objectives Develop budget plans following a zero-based approach and manage Quality costs Provide site strategy for quality management Be the Management Representative for obtaining and maintaining quality certifications (ISO 9001 etc.) Oversee execution of raw material and finished good testing and COA generation Provide site strategy and procedures for maintenance of analytical data and document control Provide strategy for in-process quality control Oversee laboratory, analytical equipment and facilities Review customer specifications and ensure that processes are capable Analyze and lead improvement efforts related to process capabilities (CpK) of production processes to eliminate product defects Focal point for site customer complaint investigation and response processes Ensure EHS compliance and continuous improvement in EHS performance Assure a compliant quality operation (incl. e.g. Responsible Care, ISO 9001/14001) Manage QA aspects of the site MOC process for pharma and non-pharma operations. Create and improve customer engagement touchpoints for matters related to product quality and regulatory compliance Assess and evaluate supplier quality processes to ensure alignment with SI quality standards; apply corrective action accordingly Oversee audit and investigation processes related to quality and for corrective measures to achieve and maintain compliance Evaluate and improve quality process work plans to reduce product rejection rates Assure the operation, maintaining, and improvements of the site's GMP and MOC processes Maintain FDA export certifications for regulatory bodies world-wide (US, Canada, EU, Mexico, Brazil, Japan) when applicable Active participation in any regional QA associated initiatives (internal/external) Serve as member of Site Leadership Team Work with other functional leaders to identify and solve problems to support achievement of site goals Anticipate future requirements for site and develop strategic plans to meet them Creating Extraordinary Starts With: Bachelor's degree in Chemistry or Chemical Engineering, or other STEM discipline Minimum of ten years' experience in process industry manufacturing Minimum of five years Supervisory experience Deep level of chemistry knowledge with training in analytical chemistry and experience in raw material and finished good testing, in-process quality control, Quality Certification Management, quality auditing quality statistics ISO 9001, 1400, RC1400 knowledge certification; ISO Auditor; cGMP certifications preferred What We Value: We strive for all employees to nurture physical, mental and emotional health both personally and professionally. Our commitment to health and wellness centers around prevention, early detection and embracing a healthy lifestyle. Some offerings may vary by role or region, but may include: Physical Health benefits including competitive Medical, Dental, and Vision packages, company contribution to Health Savings Account, cash incentive for Annual Physical and reimbursement Financial Wellness opportunities including company paid life insurance and disability plans, 401(k) Retirement Plan with generous company match, and certified Financial Planning & Investment services Mental Health benefits including generous Paid Time Off and 10 Paid Holidays, Paid Parental Bonding Leave, and much more! Company Essential Solutions with Extraordinary Results SI Group is a global leader in the innovative technology of performance additives, process solutions, active pharmaceutical ingredients, and chemical intermediates. Our solutions are essential to many diverse industries and applications, creating extraordinary results. We drive value by enhancing the quality, performance, and durability of countless items we use every day. We are on a journey to captivate our customers at every level. Whether that means expanding our capabilities, global reach, or providing new innovations and technologies that create value. Our approach is customized to exceed customer needs and deliver superior performance.
Salary Min
Salary Max
Salary Currency
Salary Periodday
Source URLhttps://hccg.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX/job/1430
Apply URLhttps://hccg.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX/job/1430
First Seen At2026-05-31 17:55:52Z
Last Seen At2026-06-06 11:05:09Z
Last Checked At2026-06-06 11:05:09Z
Last Changed At2026-05-31 17:55:52Z
Inactive At
Source Posted At2026-03-30 16:20:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hccg.fa.us2.oraclecloud.com|CX/date=2026-06-06/2026-06-06T11-05-06-637Z-c2285f517de31a919b258d90f8445cdbd801fc489adfa6351a48ec9886031a82.json
Event Fields
{
  "content_hash": "9f6d287b51409890f6eee7c00f318228de99267b7dd649a7ffa639409211fd93",
  "source_hash": "d1a098bb1cb83905a3ac45090dc2418970c4d476c5ddc53324a2488102aec3e1",
  "last_changed_at": "2026-05-31T17:55:52.864Z",
  "active_status": "active"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "Freeport, TX, United States",
    "city": "Freeport",
    "region": "TX",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T11:05:09.537Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Freeport, TX, United States",
      "city": "Freeport",
      "region": "TX",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": "day",
  "workplace_type": null,
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "detail": {
    "Id": "1430",
    "Title": "Quality Manager",
    "media": [],
    "skills": [],
    "JobType": null,
    "Category": null,
    "JobGrade": null,
    "JobLevel": null,
    "JobShift": null,
    "WorkDays": null,
    "WorkHours": null,
    "WorkYears": null,
    "Department": null,
    "HotJobFlag": false,
    "StudyLevel": null,
    "WorkMonths": null,
    "WorkerType": null,
    "GeographyId": 300000003082030,
    "JobFamilyId": null,
    "JobFunction": "Manufacturing",
    "JobSchedule": "Full time",
    "BusinessUnit": null,
    "ContractType": null,
    "Organization": null,
    "TrendingFlag": false,
    "workLocation": [
      {
        "Country": "US",
        "Region1": null,
        "Region2": "TX",
        "Region3": null,
        "Building": null,
        "Latitude": "28.98659",
        "Longitude": "-95.33906",
        "LocationId": 100000000260611,
        "PostalCode": "77541",
        "TownOrCity": "Freeport",
        "AddressLine1": "702 FM 523",
        "AddressLine2": null,
        "AddressLine3": null,
        "AddressLine4": null,
        "LocationName": "Freeport"
      }
    ],
    "ContentLocale": "en",
    "HiringManager": null,
    "LegalEmployer": null,
    "RequisitionId": 300000081817797,
    "WorkplaceType": "",
    "BusinessUnitId": 100000000260559,
    "OrganizationId": 100000000260559,
    "GeographyNodeId": 100000257740491,
    "JobFunctionCode": "MFG",
    "LegalEmployerId": 300000002434001,
    "PrimaryLocation": "Freeport, TX, United States",
    "RequisitionType": "Professional",
    "NumberOfOpenings": null,
    "WorkplaceTypeCode": null,
    "BeFirstToApplyFlag": false,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ExternalContactName": null,
    "ShortDescriptionStr": "The Quality Manager will ensure that the site meets Global Management Practices (GMP), compliance and regulatory standards. You will maintain the site in compliance with IS0 9001 standard are manufactured under GMP regulations and all shipped pharma products are of good quality.",
    "ExternalContactEmail": null,
    "ExternalPostedEndDate": null,
    "OtherRequisitionTitle": null,
    "requisitionFlexFields": [],
    "ApplyWhenNotPostedFlag": true,
    "DomesticTravelRequired": null,
    "ExternalDescriptionStr": "<p><strong>The Role:</strong></p><p>The Quality Manager will ensure that the site meets GMP, compliance and regulatory standards. You will maintain the site in compliance with IS0 9001 standard are manufactured under GMP regulations and all shipped pharma products are of good quality.</p><p><strong>How You Will Make an Impact:</strong></p><ul><li>Ensure EHS compliance and continuous improvement in EHS performance</li><li>Ensure department goals and KPIs are aligned with site objectives</li><li>Develop budget plans following a zero-based approach and manage Quality costs</li><li>Provide site strategy for quality management</li><li>Be the Management Representative for obtaining and maintaining quality certifications (ISO 9001 etc.)</li><li>Oversee execution of raw material and finished good testing and COA generation</li><li>Provide site strategy and procedures for maintenance of analytical data and document control</li><li>Provide strategy for in-process quality control</li><li>Oversee laboratory, analytical equipment and facilities</li><li>Review customer specifications and ensure that processes are capable</li><li>Analyze and lead improvement efforts related to process capabilities (CpK) of production processes to eliminate product defects</li><li>Focal point for site customer complaint investigation and response processes</li><li>Ensure EHS compliance and continuous improvement in EHS performance</li><li>Assure a compliant quality operation (incl. e.g. Responsible Care, ISO 9001/14001)</li><li>Manage QA aspects of the site MOC process for pharma and non-pharma operations.</li><li>Create and improve customer engagement touchpoints for matters related to product quality and regulatory compliance</li><li>Assess and evaluate supplier quality processes to ensure alignment with SI quality standards; apply corrective action accordingly</li><li>Oversee audit and investigation processes related to quality and for corrective measures to achieve and maintain compliance</li><li>Evaluate and improve quality process work plans to reduce product rejection rates</li><li>Assure the operation, maintaining, and improvements of the site's GMP and MOC processes</li><li>Maintain FDA export certifications for regulatory bodies world-wide (US, Canada, EU, Mexico, Brazil, Japan) when applicable</li><li>Active participation in any regional QA associated initiatives (internal/external)</li><li>Serve as member of Site Leadership Team</li><li>Work with other functional leaders to identify and solve problems to support achievement of site goals</li><li>Anticipate future requirements for site and develop strategic plans to meet them</li></ul><p><strong>Creating Extraordinary Starts With:</strong></p><ul><li>Bachelor's degree in Chemistry or Chemical Engineering, or other STEM discipline</li><li>Minimum of ten years' experience in process industry manufacturing</li><li>Minimum of five years Supervisory experience</li><li>Deep level of chemistry knowledge with training in analytical chemistry and experience in raw material and finished good testing, in-process quality control, Quality Certification Management, quality auditing quality statistics</li><li>ISO 9001, 1400, RC1400 knowledge certification; ISO Auditor; cGMP certifications preferred</li></ul><p><strong>What We Value:</strong></p><p>We strive for all employees to nurture physical, mental and emotional health both personally and professionally. Our commitment to health and wellness centers around prevention, early detection and embracing a healthy lifestyle. Some offerings may vary by role or region, but may include:&nbsp;</p><ul><li><strong>Physical Health benefits</strong>&nbsp;including competitive Medical, Dental, and Vision packages, company contribution to Health Savings Account, cash incentive for Annual Physical and reimbursement</li><li><strong>Financial Wellness opportunities</strong>&nbsp;including company paid life insurance and disability plans, 401(k) Retirement Plan with generous company match, and certified Financial Planning &amp; Investment services</li><li><strong>Mental Health benefits&nbsp;</strong>including generous Paid Time Off and 10 Paid Holidays, Paid Parental Bonding Leave, and much more! &nbsp;&nbsp;</li></ul>",
    "ObjectVerNumberProfile": "1",
    "PrimaryLocationCountry": "US",
    "CorporateDescriptionStr": "<b>Essential Solutions with Extraordinary Results</b><span></span> \n<p style=\"box-sizing: border-box; margin: 0px 0px 20px; padding: 0px; border: 0px\"><span style=\"box-sizing: border-box; margin: 0px; padding: 0px; border: 0px; font-style: inherit; font-weight: inherit\">SI Group is a global leader in the innovative technology of performance additives, process solutions, active pharmaceutical ingredients, and chemical intermediates.&nbsp;</span><span style=\"box-sizing: border-box; margin: 0px; padding: 0px; border: 0px; font-style: inherit; font-weight: inherit\">Our solutions are essential to many diverse industries and applications, creating extraordinary results. We drive value by enhancing the quality, performance, and durability of countless items we use every day.&nbsp;</span></p> \n<p style=\"box-sizing: border-box; margin: 0px 0px 20px; padding: 0px; border: 0px\"><span style=\"box-sizing: border-box; margin: 0px; padding: 0px; border: 0px; font-style: inherit; font-weight: inherit\">We are on a journey to captivate our customers at every level. Whether that means expanding our capabilities, global reach, or providing new innovations and technologies that create value. Our approach is customized to exceed customer needs and deliver superior performance.</span></p>",
    "ExternalPostedStartDate": "2026-03-30T16:20:00+00:00",
    "ExternalQualificationsStr": "",
    "InternalQualificationsStr": "",
    "OrganizationDescriptionStr": "",
    "primaryLocationCoordinates": [
      {
        "Latitude": "28.94973",
        "Longitude": "-95.3443",
        "CountryCode": "US",
        "GeographyId": 300000003082030,
        "GeographyNodeId": 100000257740491
      }
    ],
    "ExternalResponsibilitiesStr": "",
    "InternalResponsibilitiesStr": "",
    "InternationalTravelRequired": null
  },
  "list_job": {
    "Id": "1430",
    "Title": "Quality Manager",
    "JobType": null,
    "Distance": 1774828800000,
    "JobShift": null,
    "Language": "US",
    "WorkDays": null,
    "JobFamily": null,
    "Relevancy": 2,
    "WorkHours": null,
    "Department": null,
    "HotJobFlag": false,
    "PostedDate": "2026-03-30",
    "StudyLevel": null,
    "WorkerType": null,
    "GeographyId": 300000003082030,
    "JobFunction": null,
    "JobSchedule": null,
    "BusinessUnit": null,
    "ContractType": null,
    "ManagerLevel": null,
    "Organization": null,
    "TrendingFlag": false,
    "workLocation": [
      {
        "Country": "US",
        "Region1": null,
        "Region2": "TX",
        "Region3": null,
        "Building": null,
        "Latitude": 28.98659,
        "Longitude": -95.33906,
        "LocationId": 100000000260611,
        "PostalCode": "77541",
        "TownOrCity": "Freeport",
        "AddressLine1": "702 FM 523",
        "AddressLine2": null,
        "AddressLine3": null,
        "AddressLine4": null,
        "LocationName": "Freeport"
      }
    ],
    "LegalEmployer": null,
    "MediaThumbURL": null,
    "WorkplaceType": "",
    "BusinessUnitId": 100000000260559,
    "OrganizationId": 100000000260559,
    "PostingEndDate": null,
    "LegalEmployerId": 300000002434001,
    "PrimaryLocation": "Freeport, TX, United States",
    "WorkDurationYears": null,
    "WorkplaceTypeCode": null,
    "BeFirstToApplyFlag": false,
    "WorkDurationMonths": null,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ShortDescriptionStr": "The Quality Manager will ensure that the site meets Global Management Practices (GMP), compliance and regulatory standards. You will maintain the site in compliance with IS0 9001 standard are manufactured under GMP regulations and all shipped pharma products are of good quality.",
    "requisitionFlexFields": [],
    "DomesticTravelRequired": null,
    "PrimaryLocationCountry": "US",
    "ExternalQualificationsStr": null,
    "ExternalResponsibilitiesStr": null,
    "InternationalTravelRequired": null
  },
  "detail_meta": {
    "url": "https://hccg.fa.us2.oraclecloud.com/hcmRestApi/resources/latest/recruitingCEJobRequisitionDetails?expand=all&onlyData=true&finder=ById;Id=%221430%22,siteNumber=CX",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 8819
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/c3c063494c0d6948c668cc4dffd61ac3f64dd645?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/e5efa4f0-3d01-4911-bb0e-446eda2c8723JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/75bb0d91-4a48-4a97-b769-106bf2f05b05JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/c3c063494c0d6948c668cc4dffd61ac3f64dd645/eventsJSON