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HomeCompanies0d986324 3b72 4320 8897 Ce85b3aa5b54 19000101 0000012nd shift Quality/Compliance Auditor: 4-10's

2nd shift Quality/Compliance Auditor: 4-10's

0d986324 3b72 4320 8897 Ce85b3aa5b54 19000101 000001 · Montague, MI, US, Montague, MI · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
Company0d986324 3b72 4320 8897 Ce85b3aa5b54 19000101 000001
Title2nd shift Quality/Compliance Auditor: 4-10's
Normalized title-
Department / team-
LocationMontague, MI, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-06-05 / 2026-06-06
Changed / last seen2026-06-18 / 2026-06-18

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PageWhat it containsOpen
Company jobsActive postings from 0d986324 3b72 4320 8897 Ce85b3aa5b54 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 Montague.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

Company0d986324 3b72 4320 8897 Ce85b3aa5b54 19000101 000001
Sourcee3a05db3-4a76-4104-bfd8-271b8003f991
ATS providerADP Workforce Now Recruiting

Description

If you have an eye for detail, a passion for compliance, and a commitment to quality excellence, we'd like to meet you. Join a team where your expertise in GMP compliance, auditing, and quality systems directly contributes to product safety and regulatory success. We are looking for someone to join our 2nd shift team! The hours are Monday-Thursday, 3:00 PM-1:00 AM. POSITION SUMMARY: Responsible for the enforcement of Tower Laboratories, Ltd. quality system. Conduct audits related to all aspects involved in the production of drugs, medical devices, and non-drug products manufactured at Tower Laboratories to ensure cGMP compliance and production of quality product. ESSENTIAL FUNCTIONS: Perform product manufacturing audits throughout process through observation and by conducting in-process testing to ensure product meets specifications. Conduct packaging audit ensuring final product meets packaging specifications and is within the allowed accepted quality limits (AQL); inspect all incoming packaging components, ensuring specifications are met by performing appropriate tests following determined component specifications. Conduct investigations as directed and collect information to assess root causes when product or processes are not meeting specifications. Assist in the conduct of internal audits of cGMP to ensure compliance to cGMP and internal procedures and policies. Audit finished/completed batch production documents for procedural or mathematical errors prior to final review and release of product by the QA Manager. Communicate identified manufacturing deficiencies to key personnel (Machine Operator, QA Manager, Technical Director, Production Manager, & VP of Operations). Verify that all instrumentation used are calibrated and perform equipment calibrations as identified. Work as a team member; be cooperative with all departments and staff to meet company objectives. Perform all work in accordance with established Safety, cGMP and company procedures. Other responsibilities as assigned. ESSENTIAL SKILLS AND EXPERIENCE: Minimum of 2 years of pharmaceutical experience, in the Quality Assurance or Regulatory field. Demonstrated current knowledge of cGMP regulations and industry standards. Working knowledge of MS Word and MS Excel. Ability to read and follow directions, complete paperwork and communicate effectively in English. Strong writing skills. Excellent organizational skills; strong attention to detail. Good interpersonal skills; ability to communicate effectively with all levels of plant personnel. Strong team player, demonstrated team attitude and behaviors. EDUCATION: High school diploma or equivalent. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law .

Full job record

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Source IDe3a05db3-4a76-4104-bfd8-271b8003f991
Board IDe3a05db3-4a76-4104-bfd8-271b8003f991
Provideradp_workforcenow
Provider Job Key581284
Title2nd shift Quality/Compliance Auditor: 4-10's
Normalized Title
Statusactive
Activeyes
Location TextMontague, MI, US, Montague, MI
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionMI
CityMontague
Salary Raw
Salary Min
Salary Max
Salary Currency
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Source URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=0d986324-3b72-4320-8897-ce85b3aa5b54&ccId=19000101_000001&lang=en_US&type=JS&jobId=581284&jwId=9206267571746_1
Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=0d986324-3b72-4320-8897-ce85b3aa5b54&ccId=19000101_000001&lang=en_US&type=JS&jobId=581284&jwId=9206267571746_1
First Seen At2026-06-06 13:27:46Z
Last Seen At2026-06-18 13:37:13Z
Last Checked At2026-06-18 13:37:13Z
Last Changed At2026-06-18 13:37:13Z
Inactive At
Source Posted At2026-06-05 16:02:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=0d986324-3b72-4320-8897-ce85b3aa5b54|19000101_000001/date=2026-06-18/2026-06-18T13-37-13-251Z-f1f5ff952b3aec501490885b2fa0348010098c9a5ad85ce06bafd8d09b2adfb1.json
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    "requisitionDescription": "<div><div><strong><span style=\"font-size: 16px; color: rgb(40, 50, 78); font-family: arial, sans-serif;\">If you have an eye for detail, a passion for compliance, and a commitment to quality excellence, we&#39;d like to meet you.</span></strong><span style=\"color: rgb(40, 50, 78); font-size: 16px; font-family: arial, sans-serif;\"><strong>&nbsp;</strong></span><span style=\"font-family: arial, sans-serif; color: rgb(40, 50, 78);\"><strong><span style=\"font-size: 16px;\"><strong>Join a team where your expertise in GMP compliance, auditing, and quality systems directly contributes to product safety and regulatory success.</strong></span><span style=\"font-size: 18px;\"><br></span></strong><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.43.16/styles/froala_style.min.css\" rel=\"stylesheet\" type=\"text/css\"></span><div class=\"fr-view\"><div><span style=\"font-family: arial, sans-serif; color: rgb(40, 50, 78);\"><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\"><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_style.min.css\" rel=\"stylesheet\" type=\"text/css\"></span><div class=\"fr-view\"><div><span style=\"font-family: arial, sans-serif; color: rgb(40, 50, 78);\"><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\"><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_style.min.css\" rel=\"stylesheet\" type=\"text/css\"></span><div class=\"fr-view\"><p><span style=\"font-family: arial, sans-serif; color: rgb(40, 50, 78);\"><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.39.8/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\"></span><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\"><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.11.23/styles/froala_style.min.css\" rel=\"stylesheet\" type=\"text/css\"></span></p><div class=\"fr-view\"><div><div><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\"><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/22.11.23/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\"></span><p id=\"isPasted\"><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\"><strong>We are looking for someone to join our 2nd shift team! The hours are Monday-Thursday, 3:00 PM-1:00 AM.</strong></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 16px; color: rgb(40, 50, 78);\"><strong>POSITION SUMMARY:</strong></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Responsible for the enforcement of Tower Laboratories, Ltd. quality system. Conduct audits related to all aspects involved in the production of drugs, medical devices, and non-drug products manufactured at Tower Laboratories to ensure cGMP compliance and production of quality product.</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 16px; color: rgb(40, 50, 78);\"><strong>ESSENTIAL FUNCTIONS:</strong></span></p><ul type=\"disc\"><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Perform product manufacturing audits throughout process through observation and by conducting in-process testing to ensure product meets specifications. &nbsp;</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Conduct packaging audit ensuring final product meets packaging specifications and is within the allowed accepted quality limits (AQL); inspect all incoming packaging components, ensuring specifications are met by performing appropriate tests following determined component specifications.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Conduct investigations as directed and collect information to assess root causes when product or processes are not meeting specifications.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Assist in the conduct of internal audits of cGMP to ensure compliance to cGMP and internal procedures and policies.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Audit finished/completed batch production documents for procedural or mathematical errors prior to final review and release of product by the QA Manager.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Communicate identified manufacturing deficiencies to key personnel (Machine Operator, QA Manager, Technical Director, Production Manager, &amp; VP of Operations). &nbsp;</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Verify that all instrumentation used are calibrated and perform equipment calibrations as identified.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Work as a team member; be cooperative with all departments and staff to meet company objectives.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Perform all work in accordance with established Safety, cGMP and company procedures.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Other responsibilities as assigned.</li></ul><p><span style=\"font-family: arial, sans-serif; font-size: 16px; color: rgb(40, 50, 78);\"><strong>ESSENTIAL SKILLS AND EXPERIENCE:</strong></span></p><ul><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Minimum of 2 years of pharmaceutical experience, in the Quality Assurance or Regulatory field.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Demonstrated current knowledge of cGMP regulations and industry standards.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Working knowledge of MS Word and MS Excel.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Ability to read and follow directions, complete paperwork and communicate effectively in English.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Strong writing skills.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Excellent organizational skills; strong attention to detail.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Good interpersonal skills; ability to communicate effectively with all levels of plant personnel.</li><li style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">Strong team player, demonstrated team attitude and behaviors.</li></ul><p><span style=\"font-family: arial, sans-serif; font-size: 16px; color: rgb(40, 50, 78);\"><strong>EDUCATION:</strong></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\">High school diploma or equivalent.</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(40, 50, 78);\"><em><strong>We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law</strong></em></span><strong><span style=\"font-family: arial, sans-serif; font-size: 14px;\"><strong><span style=\"color: rgb(40, 50, 78);\">.</span></strong></span></strong></p></div></div></div><p><br></p></div></div></div></div></div></div></div>\n",
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