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Home › Companies › Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003 › MANAGER, QUALITY ASSURANCE

MANAGER, QUALITY ASSURANCE

Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003 · Taylor, MS, US, Taylor, MS · Active · $95,000–$110,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyFbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003
TitleMANAGER, QUALITY ASSURANCE
Normalized title-
Department / team-
LocationTaylor, MS, United States
Work model-
Employment typeFull Time
Salary$95,000–$110,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-06-02 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003.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 Taylor.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

CompanyFbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003
Sourcee088055a-0c65-47db-aa4c-74f9b0047486
ATS providerADP Workforce Now Recruiting

Description

RESPONSIBILITIES : Supervise daily warehouse operations to ensure efficient material flow and timely completion of Quality Assurance activities Provide oversight of quality systems, including labeling, GMP training, compliance, document control, information tracking, and equipment calibration Lead investigation activities, perform root cause analysis, and develop corrective and preventive action (CAPA) plans Support internal and external audits and regulatory inspections, ensuring timely resolution and closure of findings Develop, maintain, and control document storage and retrieval systems in compliance with GMP requirements Review and approve Quality Operations processes, SOPs, and GMP documentation, as applicable Utilize statistical process control to analyze quality trends and prepare KPI reports for senior management Ensure timely closure and effective management of audit findings Prepare QA reports and provide data to support cross-functional business needs Oversee management of deviations, CAPAs, and change controls in a timely and compliant manner Support customer complaint investigations, ensuring appropriate documentation and resolution Supervise, train, and mentor junior QA staff to support team development and capability building Ensure full compliance with cGMP regulations and all applicable SOPs Experience in Active Pharmaceutical Ingredient (API) environments Experience in quality operations within manufacturing, warehouse, and supply chain environments Exposure to international supply chain and distribution operations preferred Strong knowledge of Quality Systems and GMP compliance requirements Hands-on experience with vendor management, customer complaints, deviations, CAPA, change control, and investigations Experience supporting internal and external audits and regulatory inspections Knowledge of document control systems, GMP training programs, labeling systems, and metrology programs QUALIFICATIONS: Bachelor’s degree in a scientific discipline 10+ years of experience in Quality Assurance within a GMP-regulated manufacturing environment, or equivalent combination of education and experience 5+ years of experience in a supervisory or leadership role within a GMP-regulated manufacturing or distribution environment preferred Ability to read and interpret technical procedures, SOPs, GMP regulations, and governmental requirements Strong written and verbal communication skills Ability to organize, prioritize, and manage multiple tasks with minimal supervision High attention to detail and strong analytical skills Knowledge of ICH Q7, 21 CFR Part 11, and 21 CFR 210 & 211 ASQ certifications, ISO 9000 knowledge, or formal audit training preferred. At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

Full job record

Job ID4f2ed7bd82a19646004c506e43577121f0146d7a
Org ID1c12f03c-6518-4018-9e8a-db5c3c140f34
Source IDe088055a-0c65-47db-aa4c-74f9b0047486
Board IDe088055a-0c65-47db-aa4c-74f9b0047486
Provideradp_workforcenow
Provider Job Key516134
TitleMANAGER, QUALITY ASSURANCE
Normalized Title—
Statusactive
Activeyes
Location TextTaylor, MS, US, Taylor, MS
Department—
Team—
Employment Typefull_time
Workplace Type—
Remote Policy—
CountryUnited States
RegionMS
CityTaylor
Salary Raw95000.00 To 110000.00 (USD) Annually
Salary Min95,000
Salary Max110,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=fbb6193d-556c-4b29-98e5-7306aa3f6384&ccId=19000101_000003&lang=en_US&type=JS&jobId=516134&jwId=9200835284257_1
Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=fbb6193d-556c-4b29-98e5-7306aa3f6384&ccId=19000101_000003&lang=en_US&type=JS&jobId=516134&jwId=9200835284257_1
First Seen At2026-05-31 18:58:01Z
Last Seen At2026-06-06 12:58:45Z
Last Checked At2026-06-06 12:58:45Z
Last Changed At2026-06-06 12:58:45Z
Inactive At—
Source Posted At2026-06-02 21:46:00Z
Source Updated At—
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=fbb6193d-556c-4b29-98e5-7306aa3f6384|19000101_000003/date=2026-06-06/2026-06-06T12-58-44-922Z-ddd9671f0b308db51448c9dbd528c5c83a531bc0232614a44d7aa5a0b50736e4.json
Event Fields
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Parsed Structured
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  "salary_period": "year",
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Extensions
{}
Native Structured
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    "requisitionDescription": "<div><div><div><div><div><div><h2 data-section-id=\"egncad\" data-start=\"98\" data-end=\"122\" data-pasted=\"true\"><strong data-start=\"101\" data-end=\"122\"><span style=\"font-size: 16px;\">RESPONSIBILITIES</span>:</strong></h2><ul data-start=\"124\" data-end=\"1487\"><li data-section-id=\"fpe504\" data-start=\"124\" data-end=\"252\">Supervise daily warehouse operations to ensure efficient material flow and timely completion of Quality Assurance activities</li><li data-section-id=\"1mf8h7i\" data-start=\"253\" data-end=\"406\">Provide oversight of quality systems, including labeling, GMP training, compliance, document control, information tracking, and equipment calibration</li><li data-section-id=\"8cfx2\" data-start=\"407\" data-end=\"528\">Lead investigation activities, perform root cause analysis, and develop corrective and preventive action (CAPA) plans</li><li data-section-id=\"15vl9m6\" data-start=\"529\" data-end=\"648\">Support internal and external audits and regulatory inspections, ensuring timely resolution and closure of findings</li><li data-section-id=\"19v4evz\" data-start=\"649\" data-end=\"758\">Develop, maintain, and control document storage and retrieval systems in compliance with GMP requirements</li><li data-section-id=\"sajg3z\" data-start=\"759\" data-end=\"854\">Review and approve Quality Operations processes, SOPs, and GMP documentation, as applicable</li><li data-section-id=\"x76d5w\" data-start=\"855\" data-end=\"966\">Utilize statistical process control to analyze quality trends and prepare KPI reports for senior management</li><li data-section-id=\"iu53wk\" data-start=\"967\" data-end=\"1035\">Ensure timely closure and effective management of audit findings</li><li data-section-id=\"vexwvv\" data-start=\"1036\" data-end=\"1118\">Prepare QA reports and provide data to support cross-functional business needs</li><li data-section-id=\"byqja7\" data-start=\"1119\" data-end=\"1216\">Oversee management of deviations, CAPAs, and change controls in a timely and compliant manner</li><li data-section-id=\"viiokc\" data-start=\"1217\" data-end=\"1313\">Support customer complaint investigations, ensuring appropriate documentation and resolution</li><li data-section-id=\"1mdy2kg\" data-start=\"1314\" data-end=\"1414\">Supervise, train, and mentor junior QA staff to support team development and capability building</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Ensure full compliance with cGMP regulations and all applicable SOPs</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Experience in Active Pharmaceutical Ingredient (API) environments</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Experience in quality operations within manufacturing, warehouse, and supply chain environments</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Exposure to international supply chain and distribution operations preferred</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Strong knowledge of Quality Systems and GMP compliance requirements</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Hands-on experience with vendor management, customer complaints, deviations, CAPA, change control, and investigations</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Experience supporting internal and external audits and regulatory inspections</li><li data-section-id=\"hgnraw\" data-start=\"1415\" data-end=\"1487\">Knowledge of document control systems, GMP training programs, labeling systems, and metrology programs</li></ul><h2 data-section-id=\"1r8ofct\" data-start=\"2164\" data-end=\"2186\"><strong data-start=\"2167\" data-end=\"2186\"><span style=\"font-size: 16px;\">QUALIFICATIONS:</span></strong></h2><ul data-start=\"2188\" data-end=\"2974\"><li data-section-id=\"ulp011\" data-start=\"2188\" data-end=\"2236\">Bachelor&rsquo;s degree in a scientific discipline</li><li data-section-id=\"1768jid\" data-start=\"2237\" data-end=\"2389\">10+ years of experience in Quality Assurance within a GMP-regulated manufacturing environment, or equivalent combination of education and experience</li><li data-section-id=\"16t6tqz\" data-start=\"2390\" data-end=\"2527\">5+ years of experience in a supervisory or leadership role within a GMP-regulated manufacturing or distribution environment preferred</li><li data-section-id=\"y0at2b\" data-start=\"2528\" data-end=\"2636\">Ability to read and interpret technical procedures, SOPs, GMP regulations, and governmental requirements</li><li data-section-id=\"1syne7v\" data-start=\"2637\" data-end=\"2687\">Strong written and verbal communication skills</li><li data-section-id=\"1gxgx8v\" data-start=\"2688\" data-end=\"2775\">Ability to organize, prioritize, and manage multiple tasks with minimal supervision</li><li data-section-id=\"mua8vc\" data-start=\"2776\" data-end=\"2833\">High attention to detail and strong analytical skills</li><li data-section-id=\"ivhbbg\" data-start=\"2834\" data-end=\"2895\">Knowledge of ICH Q7, 21 CFR Part 11, and 21 CFR 210 &amp; 211</li><li data-section-id=\"2nc4w0\" data-start=\"2896\" data-end=\"2974\">ASQ certifications, ISO 9000 knowledge, or formal audit training preferred.&nbsp;</li></ul><p data-pasted=\"true\" style='box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; line-height: 1.25; margin: 0px 0px 16px; font-size: 16px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; padding: 0px; color: rgb(51, 51, 51); font-family: \"Trebuchet MS\", \"Helvetica Neue\", Helvetica, Tahoma, sans-serif;'>At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer.</p><p style='box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; line-height: 1.25; margin: 0px 0px 16px; font-size: 16px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; padding: 0px; color: rgb(51, 51, 51); font-family: \"Trebuchet MS\", \"Helvetica Neue\", Helvetica, Tahoma, sans-serif;'>All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.</p><p style=\"box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; line-height: 1.25; margin-top: 0px; margin-bottom: 1rem;\"><br style=\"box-sizing: border-box; outline: none; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; color: rgb(38, 35, 33); font-family: Circular, -apple-system, BlinkMacSystemFont, &quot;Segoe UI&quot;, Roboto, Oxygen, Ubuntu, Cantarell, &quot;Fira Sans&quot;, &quot;Droid Sans&quot;, &quot;Helvetica Neue&quot;, sans-serif; font-size: 16px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;\"></p></div></div></div></div></div></div>\n",
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