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Home › Companies › 2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 › QA Compliance Specialist II

QA Compliance Specialist II

2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 · Lee, MA, US, Lee, MA · Active · $65,000–$85,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001
TitleQA Compliance Specialist II
Normalized title-
Department / team-
LocationLee, MA, United States
Work model-
Employment typeFull Time
Salary$65,000–$85,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-05-18 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from 2479a996 4c61 4623 Bd61 684f50d6e2a0 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 Lee.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

Company2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001
Source95b4d553-a046-4c74-bcb4-9264e4e35c82
ATS providerADP Workforce Now Recruiting

Description

Position Summary The QA Compliance Specialist II is a quality professional who assists with compliance and quality activities at SSM. The QA Compliance Specialist assists with implementing cGMP and regulatory requirements at SSM. The QA Compliance Specialist is responsible for maintaining and improving the Quality Culture at SSM. Duties and Responsibilities Provide indirect oversight of cGMP operations at SSM, ensuring compliance with regulatory requirements. Work collaboratively within SSM’s Quality Management System (QMS) to support quality initiatives and continuous improvement. Author, review, and approve documentation in compliance with FDA, EU, and other applicable regulatory agency requirements. Manage and process Change Controls, Deviations, CAPAs, Work Orders, and other GMP-related documents, ensuring timely resolution and compliance. Conduct and support internal audits and routine walkthrough inspections of manufacturing areas, authoring and reviewing associated reports. Collaborate cross-functionally with other departments to achieve on-time closure of Quality Events and maintain quality standards. Assist in the execution and oversight of the Pest Control Program, ensuring compliance with facility and regulatory requirements. Maintain strong organizational skills, with the ability to efficiently review, edit, and manage documentation. Demonstrate a high level of attention to detail while managing multiple tasks and priorities. Effectively manage timelines and deliverables to meet department and organizational goals. Maintain control and confidentiality of all quality-related documents and sensitive information. Perform other duties assigned by the Quality Manager, supporting the continuous improvement of SSM’s Quality Systems. Other duties as assigned. Regulatory Responsibilities Exhibit a quality mindset Conduct business in a responsible manner that complies with FDA, EU and other regulatory agency requirements Supervisory Responsibilities N/A Experience Three (3) to five (5) years of experience working in a cGMP environment (preferably in a QA function) Education Bachelor’s Degree (relevant experience may be substituted for degree) Knowledge, Skills & Abilities Skilled in the use of Microsoft office applications (Word, Excel, PowerPoint) and Adobe Acrobat Knowledge of an electronic Quality Management System High attention to detail Good writing, public speaking, and presentation skills Physical Requirements Ability to sit for prolonged periods of time Ability to lift up to 25lbs Ability to stand for prolonged periods of time

Full job record

Job ID7d4c4b09891b09b09bf06bdfd219149fefa5967d
Org IDffbe8dfc-07e3-4259-8a85-b9f1dd382d16
Source ID95b4d553-a046-4c74-bcb4-9264e4e35c82
Board ID95b4d553-a046-4c74-bcb4-9264e4e35c82
Provideradp_workforcenow
Provider Job Key593731
TitleQA Compliance Specialist II
Normalized Title—
Statusactive
Activeyes
Location TextLee, MA, US, Lee, MA
Department—
Team—
Employment Typefull_time
Workplace Type—
Remote Policy—
CountryUnited States
RegionMA
CityLee
Salary Raw65000.00 To 85000.00 (USD) Annually
Salary Min65,000
Salary Max85,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&lang=en_US&type=JS&jobId=593731&jwId=9201151977056_1
Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&lang=en_US&type=JS&jobId=593731&jwId=9201151977056_1
First Seen At2026-05-31 18:44:29Z
Last Seen At2026-06-06 13:18:53Z
Last Checked At2026-06-06 13:18:53Z
Last Changed At2026-06-06 13:18:53Z
Inactive At—
Source Posted At2026-05-18 15:06:00Z
Source Updated At—
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    "requisitionDescription": "<div><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"720\" style=\"width:539.75pt;border-collapse:collapse;border:none;\" id=\"isPasted\"><tbody><tr><td valign=\"top\" style=\"width: 20.1669%; border: 1pt solid windowtext; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Position Summary</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: 1pt solid windowtext; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-image: initial; border-left: none; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:6.05pt;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:black;'>The QA Compliance Specialist II is a quality professional who assists with compliance and quality activities at SSM. The QA Compliance Specialist assists with implementing cGMP and regulatory requirements at SSM. The QA Compliance Specialist is responsible for maintaining and improving the Quality Culture at SSM.</span></p></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Duties and Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 10.3px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Provide indirect oversight of cGMP operations at SSM, ensuring compliance with regulatory requirements.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Work collaboratively within SSM&rsquo;s Quality Management System (QMS) to support quality initiatives and continuous improvement.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Author, review, and approve documentation in compliance with FDA, EU, and other applicable regulatory agency requirements.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Manage and process Change Controls, Deviations, CAPAs, Work Orders, and other GMP-related documents, ensuring timely resolution and compliance.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Conduct and support internal audits and routine walkthrough inspections of manufacturing areas, authoring and reviewing associated reports.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Collaborate cross-functionally with other departments to achieve on-time closure of Quality Events and maintain quality standards.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Assist in the execution and oversight of the Pest Control Program, ensuring compliance with facility and regulatory requirements.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Maintain strong organizational skills, with the ability to efficiently review, edit, and manage documentation.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Demonstrate a high level of attention to detail while managing multiple tasks and priorities.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Effectively manage timelines and deliverables to meet department and organizational goals.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Maintain control and confidentiality of all quality-related documents and sensitive information.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Perform other duties assigned by the Quality Manager, supporting the continuous improvement of SSM&rsquo;s Quality Systems.</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Other duties as assigned.</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 48.55pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Regulatory Responsibilities &nbsp;</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 48.55pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 10.3px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Exhibit a quality mindset</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Conduct business in a responsible manner that complies with FDA, EU and other regulatory agency requirements</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 23.95pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Supervisory Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 23.95pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 10.3px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;'>N/A</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 23.15pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Experience</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 23.15pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 10.3px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Three (3) to five (5) years of experience working in a cGMP environment (preferably in a QA function)</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 19.75pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Education</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 19.75pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 10.3px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Bachelor&rsquo;s Degree (relevant experience may be substituted for degree)</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 33.25pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Knowledge, Skills &amp; Abilities</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 33.25pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 10.3px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Skilled in the use of Microsoft office applications (Word, Excel, PowerPoint) and Adobe Acrobat</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Knowledge of an electronic Quality Management System</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>High attention to detail</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Good writing, public speaking, and presentation skills</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 20.1669%; border-right: 1pt solid windowtext; border-bottom: 1pt solid windowtext; border-left: 1pt solid windowtext; border-image: initial; border-top: none; padding: 0in 5.4pt; height: 30.1pt; vertical-align: top;\"><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Physical Requirements</span></strong><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'> </span></strong></p><p style='margin-right:0in;margin-left:0in;font-size:13px;font-family:\"Times New Roman\",serif;margin:0in;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#FF6600;'>&nbsp;</span></strong></p></td><td valign=\"top\" style=\"width: 79.8331%; border-top: none; border-left: none; border-bottom: 1pt solid windowtext; border-right: 1pt solid windowtext; padding: 0in 5.4pt; height: 30.1pt; vertical-align: top;\"><div style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 10.3px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Ability to sit for prolonged periods of time</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Ability to lift up to 25lbs</span></li><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:black;'>Ability to stand for prolonged periods of time</span></li></ul></div></td></tr></tbody></table></div>\n",
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}
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