Home › Companies › C651fb5d De84 4c3e A077 94f932e8382e 19000101 000001 › Quality 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
| Field | Value |
|---|---|
| Company | C651fb5d De84 4c3e A077 94f932e8382e 19000101 000001 |
| Title | Quality Control Technician |
| Normalized title | - |
| Department / team | - |
| Location | CCARE Campus, MD, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | ADP Workforce Now Recruiting |
| Posted / first seen | 2022-10-07 / 2026-05-31 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from C651fb5d De84 4c3e A077 94f932e8382e 19000101 000001. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through ADP Workforce Now Recruiting. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in CCARE Campus. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | C651fb5d De84 4c3e A077 94f932e8382e 19000101 000001 |
| Source | 06b66957-82f5-43c8-bed2-f027772b403b |
| ATS provider | ADP 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 ID | 0184d6c2-b293-40c0-bea7-003f6c00200a |
| Source ID | 06b66957-82f5-43c8-bed2-f027772b403b |
| Board ID | 06b66957-82f5-43c8-bed2-f027772b403b |
| Provider | adp_workforcenow |
| Provider Job Key | 465275 |
| Title | Quality Control Technician |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | CCARE Campus, Linthicum Heights, MD, US, Linthicum Heights, MD |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | MD |
| City | CCARE Campus |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=c651fb5d-de84-4c3e-a077-94f932e8382e&ccId=19000101_000001&lang=en_US&type=JS&jobId=465275&jwId=9200852506784_1 |
| Apply URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=c651fb5d-de84-4c3e-a077-94f932e8382e&ccId=19000101_000001&lang=en_US&type=JS&jobId=465275&jwId=9200852506784_1 |
| First Seen At | 2026-05-31 18:09:56Z |
| Last Seen At | 2026-06-06 12:14:58Z |
| Last Checked At | 2026-06-06 12:14:58Z |
| Last Changed At | 2026-06-06 12:14:58Z |
| Inactive At | — |
| Source Posted At | 2022-10-07 16:35:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=c651fb5d-de84-4c3e-a077-94f932e8382e|19000101_000001/date=2026-06-06/2026-06-06T12-14-57-985Z-e5b17eb380154e95ae5ba8d0a2024391311489997e7786211f23a0f32f3d95bf.json |
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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;'> </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;\"> </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. </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. </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. </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. </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 & orally. </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. </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. 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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=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/0184d6c2-b293-40c0-bea7-003f6c00200aJSONGET https://api.bluedoor.sh/job-postings/v1/sources/06b66957-82f5-43c8-bed2-f027772b403bJSONGET https://api.bluedoor.sh/job-postings/v1/jobs/b515d5bc8d6c74cf2ee6c991fc2102fca95a3f64/eventsJSON