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HomeCompaniesC651fb5d De84 4c3e A077 94f932e8382e 19000101 000001Quality Control Technician

Quality Control Technician

C651fb5d De84 4c3e A077 94f932e8382e 19000101 000001 · CCARE Campus, Linthicum Heights, MD, US, Linthicum Heights, MD · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyC651fb5d De84 4c3e A077 94f932e8382e 19000101 000001
TitleQuality Control Technician
Normalized title-
Department / team-
LocationCCARE Campus, MD, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2022-10-07 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from C651fb5d De84 4c3e A077 94f932e8382e 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 CCARE Campus.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

CompanyC651fb5d De84 4c3e A077 94f932e8382e 19000101 000001
Source06b66957-82f5-43c8-bed2-f027772b403b
ATS providerADP Workforce Now Recruiting

Description

NOTE: The schedule for this opportunity is Monday- Friday, 2:00 PM - 10:30 PM POSITION SUMMARY: The Quality Control Technician will assist in ensuring the manufacturing (mixing/compounding/weighing) and filling production lines generate a consistently suitable output of products that meet quality and efficiency standards. Quality Control Technicians work within the production shifts, and assist documenting, recording and maintaining critical and other quality checks within each area of the facility. ESSENTIAL FUNCTIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job. Other duties may be assigned. Assist in Quality department efforts in inspection and testing of received, and in-process materials, components, and products to ensure adherence to established quality standards. Perform quality checks including but not limited to: start-up procedures and 30-minute checks, pallet check assessments, labeling assessment, product organoleptic evaluation, and batch related information assurance. Ensure both self, and other QC technicians, as well as specialized Production employees tasked with quality tasks, all are maintaining all quality checks in accordance with the site Quality Management Program. Assist in the development of an enhanced quality control process within C-Care, to include warehouse, receiving, mixing/compounding, and filling areas. Assist Quality Control Manager, as well as Director of Quality on driving deviation reporting and non-conformity observations from all areas of the facility to Quality Assurance management, Director of Quality and production staff and management as needed. Assist in the development of a robust, communicative, and controlled quality process with the Director of Quality and Technical Services Manager. Voice and escalate concerns including quality deviations, employee safety and/or management issues, and all hazard control areas within the facility. Demonstrate proactive thinking and critical, rapid correction as needed. Assist in development and evaluation of new procedures and protocols with the Director of Quality. Verification of checklist paperwork and/or electronic records daily. Deliver quality results and recordkeeping. Attend EHS meetings and discuss potential risks and issues. Maintain critical awareness of all areas of the facility with respect to quality and hazard control. QUALIFICATIONS: B.S. or B.A. in a related field. 2+ years of prior experience in a quality control role with direct experience in observing product quality within a manufacturing process and environment. Prior experience with reviewing batch records, start-up records, 30-min checklists and all other quality documentation for verification purposes is preferred. Prior training as an ISO 22716 Lead Auditor and Internal Auditing, HACCP and FDA GMP/OTC guidelines within 21 CFR 210-2101 is a plus. Ability to work independently without supervision in a deadline-driven environment. Ability to communicate effectively with all levels of management, both written & orally. Must be detail-oriented with excellent organizational skills. Prior experience with MS Office applications like Word and Excel. Availability and willingness to work flexible hours including some nights and weekends to meet customer needs. Sampling of materials may require lifting of drum lids and/or shifting of 55lb. Bags; Lifting of 5g reagent chemical drums; walking throughout facility (140,000 sq. ft.) and climbing stairs to processing area.

Full job record

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Org ID0184d6c2-b293-40c0-bea7-003f6c00200a
Source ID06b66957-82f5-43c8-bed2-f027772b403b
Board ID06b66957-82f5-43c8-bed2-f027772b403b
Provideradp_workforcenow
Provider Job Key465275
TitleQuality Control Technician
Normalized Title
Statusactive
Activeyes
Location TextCCARE Campus, Linthicum Heights, MD, US, Linthicum Heights, MD
Department
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Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionMD
CityCCARE Campus
Salary Raw
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First Seen At2026-05-31 18:09:56Z
Last Seen At2026-06-06 12:14:58Z
Last Checked At2026-06-06 12:14:58Z
Last Changed At2026-06-06 12:14:58Z
Inactive At
Source Posted At2022-10-07 16:35:00Z
Source Updated At
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Event Fields
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    "requisitionDescription": "\n    <link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\" />\n    <link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_style.min.css\" rel=\"stylesheet\" type=\"text/css\" />\n\n    <div class=\"fr-view\">\n      <div><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\"> <div class=\"fr-view\"><div><div id=\"isPasted\" style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none windowtext 1.0pt;padding:1.0pt 3.0pt 1.0pt 3.0pt;'><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;border-bottom:0in none windowtext;'><strong id=\"isPasted\"><em><span style=\"color: rgb(44, 130, 201);\">NOTE: The schedule for this opportunity is Monday- Friday, 2:00 PM - 10:30 PM</span></em></strong></p><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;border-bottom:0in none windowtext;'><br></p><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;border-bottom:0in none windowtext;'><strong><u><span style=\"font-size:16px;line-height:115%;font-family:Roboto;color:#444444;\">POSITION SUMMARY:</span></u></strong></p><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;border-bottom:0in none windowtext;'><span style='font-size:14px;line-height:115%;font-family:\"Times New Roman\",serif;color:#444444;'>The Quality Control Technician will assist in ensuring the manufacturing (mixing/compounding/weighing) and filling production lines generate a consistently suitable output of products that meet quality and efficiency standards. Quality Control Technicians work within the production shifts, and assist documenting, recording and maintaining critical and other quality checks within each area of the facility.</span><strong><span style='font-size:14px;line-height:115%;font-family:\"Times New Roman\",serif;color:#444444;'>&nbsp;&nbsp;</span></strong></p><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;border-bottom:0in none windowtext;'><strong><span style=\"font-size:13px;line-height:115%;font-family:Roboto;color:#444444;\">&nbsp;</span></strong></p><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;border-bottom:0in none windowtext;'><strong><u><span style=\"font-size:16px;line-height:115%;font-family:Roboto;color:#444444;\">ESSENTIAL FUNCTIONS:</span></u></strong></p><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;'><span style='font-size:14px;line-height:115%;font-family:\"Times New Roman\",serif;color:#444444;'>To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job. Other duties may be assigned.</span></p></div><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none windowtext 1.0pt;padding:1.0pt 3.0pt 1.0pt 3.0pt;margin-left:.25in;margin-right:0in;'><ul style=\"list-style-type: circle; margin-left: -0.25in;\"><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;color:#444444;'>Assist in Quality department efforts in inspection and testing of received, and in-process materials, components, and products to ensure adherence to established quality standards.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Perform quality checks including but not limited to: start-up procedures and 30-minute checks, pallet check assessments, labeling assessment, product organoleptic evaluation, and batch related information assurance. &nbsp;</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Ensure both self, and other QC technicians, as well as specialized Production employees tasked with quality tasks, all are maintaining all quality checks in accordance with the site Quality Management Program. &nbsp;</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Assist in the development of an enhanced quality control process within C-Care, to include warehouse, receiving, mixing/compounding, and filling areas.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Assist Quality Control Manager, as well as Director of Quality on driving deviation reporting and non-conformity observations from all areas of the facility to Quality Assurance management, Director of Quality and production staff and management as needed.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Assist in the development of a robust, communicative, and controlled quality process with the Director of Quality and Technical Services Manager.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Voice and escalate concerns including quality deviations, employee safety and/or management issues, and all hazard control areas within the facility.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Demonstrate proactive thinking and critical, rapid correction as needed.&nbsp;</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Assist in development and evaluation of new procedures and protocols with the Director of Quality.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Verification of checklist paperwork and/or electronic records daily.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Deliver quality results and recordkeeping.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Attend EHS meetings and discuss potential risks and issues.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;color:#444444;'>Maintain critical awareness of all areas of the facility with respect to quality and hazard control.</span></li></ul></div><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none windowtext 1.0pt;padding:1.0pt 3.0pt 1.0pt 3.0pt;'><div id=\"isPasted\"><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none windowtext 1.0pt;padding:1.0pt 3.0pt 1.0pt 3.0pt;'><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none;padding:0in;border-bottom:0in none windowtext;'><strong><u><span style=\"font-size:16px;line-height:115%;font-family:Roboto;color:#444444;\">QUALIFICATIONS:</span></u></strong></p></div></div></div><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none windowtext 1.0pt;padding:1.0pt 3.0pt 1.0pt 3.0pt;margin-left:.25in;margin-right:0in;'><ul style=\"list-style-type: circle; margin-left: -0.25in;\"><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;color:#444444;'>B.S. or B.A. in a related field.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>2+ years of prior experience in a quality control role with direct experience in observing product quality within a manufacturing process and environment.&nbsp;</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Prior experience with reviewing batch records, start-up records, 30-min checklists and all other quality documentation for verification purposes is preferred.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Prior training as an ISO 22716 Lead Auditor and Internal Auditing, HACCP and FDA GMP/OTC guidelines within 21 CFR 210-2101 is a plus.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Ability to work independently without supervision in a deadline-driven environment.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Ability to communicate effectively with all levels of management, both written &amp; orally.&nbsp;</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Must be detail-oriented with excellent organizational skills.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Prior experience with MS Office applications like Word and Excel.</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;font-family:\"Times New Roman\",serif;font-size:10.5pt;color:#444444;'>Availability and willingness to work flexible hours including some nights and weekends to meet customer needs.&nbsp;</span></li><li><span style='line-height:115%;font-family:\"Times New Roman\",serif;color:#444444;'>Sampling of materials may require lifting of drum lids and/or shifting of 55lb. Bags; Lifting of 5g reagent chemical drums; walking throughout facility (140,000 sq. ft.) and climbing stairs to processing area.</span></li></ul></div><div style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;border:none windowtext 1.0pt;padding:1.0pt 3.0pt 1.0pt 3.0pt;'><p style='margin:0in;line-height:115%;font-size:15px;font-family:\"Arial\",sans-serif;margin-bottom:4.0pt;border:none;padding:0in;'><strong><span style=\"font-size:19px;line-height:115%;font-family:Roboto;color:#444444;\">&nbsp;</span></strong></p></div></div></div></div>\n    </div>\n  \n",
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Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/b515d5bc8d6c74cf2ee6c991fc2102fca95a3f64?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/0184d6c2-b293-40c0-bea7-003f6c00200aJSON
GET https://api.bluedoor.sh/job-postings/v1/sources/06b66957-82f5-43c8-bed2-f027772b403bJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/b515d5bc8d6c74cf2ee6c991fc2102fca95a3f64/eventsJSON