Home › Companies › 2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 › Director of Quality Operations
Director of Quality Operations
2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 · Lee, MA, US, Lee, MA · Deleted · $90,000–$160,000 / year · ADP Workforce Now Recruiting
Job facts
| Field | Value |
|---|---|
| Company | 2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 |
| Title | Director of Quality Operations |
| Normalized title | - |
| Department / team | - |
| Location | Lee, MA, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | $90,000–$160,000 / year |
| Status | deleted |
| ATS provider | ADP Workforce Now Recruiting |
| Posted / first seen | 2026-02-10 / 2026-05-31 |
| Changed / last seen | 2026-06-04 / 2026-06-02 |
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| Page | What it contains | Open |
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| Company jobs | Active postings from 2479a996 4c61 4623 Bd61 684f50d6e2a0 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 Lee. | 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 | 2479a996 4c61 4623 Bd61 684f50d6e2a0 19000101 000001 |
| Source | 95b4d553-a046-4c74-bcb4-9264e4e35c82 |
| ATS provider | ADP Workforce Now Recruiting |
Description
Position Summary
The Director of Quality Operations is a critical leadership position responsible for ensuring the highest standards of quality and compliance in the sterile drug manufacturing process. This individual will lead and oversee key quality operations functions, while ensuring alignment with customer & regulatory requirements and company objectives. The role requires a blend of technical expertise, analytical thinking, and leadership skills to address challenges, optimize processes, foster a culture of continuous improvement across the organization and enhance client relationships.
Duties and Responsibilities
Ensure compliance with cGMP, FDA, and other applicable regulatory requirements for sterile drug manufacturing. Lead the team in quality oversight of manufacturing processes, ensuring adherence to SOPs and quality standards. Drive initiatives to strengthen aseptic technique, contamination control strategies, and data integrity practices. Support the development and maintenance of a robust risk management program, ensuring all critical issues are addressed with sustainable solutions. Serve as the quality operations representative during internal and external meetings with clients and other entities. Respond to client inquiries, quality concerns, and requests in a timely and professional manner. Oversee the resolution of client-related deviations, investigations, and CAPAs, ensuring timely closure. Provide root cause analysis and implement preventive measures for recurring client concerns. Lead cross-functional teams to ensure effective resolution of quality issues impacting clients. Facilitate effective communication between clients and internal stakeholders to ensure alignment on quality objectives. Travel as needed Other duties as assigned Regulatory Responsibilities
Keep abreast of changes to qua l ity regulations and guidelines, advise the management team of any bus i ness i mplications of these changes Maintain a deta il ed and comprehensive understanding of FDA, EU and other regulatory agency requ i rements Conduct all work i n compliance with FDA, 21 CFR 820, 21 CFR 210 and 211 and other regulatory agency requirements Supervisory Responsibilities
Lead and direct work and provide feedback to a team of QA Specialists Lead, manage and ensure proper training to any relevant change management programs throughout the company Experience
Eight to ten (8-10) years of progressively responsible related quality assurance experience Education
Bachelor's Degree Knowledge, Skills & Abilities
Subject matter expertise in FDA, EU, and other regulatory agency requirements Comprehensive knowledge of QA concepts and principles Knowledge of cGMP principles Knowledge of RCA tools Ability to work as part of a team Management skills Ability to manage multiple client relationships and priorities effectively Good oral and written communication Problem/situation analysis Ability to build collaborative relationships Uses good judgement Perform complex work instructions and problem solving following established processes Experience with Microsoft Office and general computer proficiency Quality mindset and a willingness to develop yourself and others Physical Requirements
Ability to remain stationary for long periods of time Ability to move between locations May occasionally lift up to 10 lbs.
Full job record
| Job ID | 72bea3f57f33093cad9ce73e608fed8f6829d59a |
| Org ID | ffbe8dfc-07e3-4259-8a85-b9f1dd382d16 |
| Source ID | 95b4d553-a046-4c74-bcb4-9264e4e35c82 |
| Board ID | 95b4d553-a046-4c74-bcb4-9264e4e35c82 |
| Provider | adp_workforcenow |
| Provider Job Key | 538421 |
| Title | Director of Quality Operations |
| Normalized Title | — |
| Status | deleted |
| Active | no |
| Location Text | Lee, MA, US, Lee, MA |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | MA |
| City | Lee |
| Salary Raw | 90000.00 To 160000.00 (USD) Annually |
| Salary Min | 90,000 |
| Salary Max | 160,000 |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&lang=en_US&type=JS&jobId=538421&jwId=9200886991440_1 |
| Apply URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=2479a996-4c61-4623-bd61-684f50d6e2a0&ccId=19000101_000001&lang=en_US&type=JS&jobId=538421&jwId=9200886991440_1 |
| First Seen At | 2026-05-31 18:44:29Z |
| Last Seen At | 2026-06-02 09:38:38Z |
| Last Checked At | 2026-06-04 09:36:19Z |
| Last Changed At | 2026-06-04 09:36:19Z |
| Inactive At | 2026-06-04 09:36:19Z |
| Source Posted At | 2026-02-10 15:12:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://bluework-jobs-prod-raw-590183727216/raw/provider=adp_workforcenow/board=2479a996-4c61-4623-bd61-684f50d6e2a0|19000101_000001/date=2026-06-02/2026-06-02T09-38-37-842Z-f9c6e468eeff549ce1b01a412bfa7af5a2dbfae6fa035270d448a89018946c37.json |
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"requisitionDescription": "<div><div><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: 26.1474%; border: 1pt solid windowtext; padding: 0in 5.4pt; height: 27.4pt; vertical-align: top;\"><p style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Position Summary</span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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-top:0in;margin-right:17.9pt;margin-bottom:.0001pt;margin-left:5.6pt;font-size:16px;font-family:\"Arial\",sans-serif;text-indent:-.1pt;'><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#181818;'>The Director of Quality Operations is a critical leadership position responsible for ensuring the highest standards of quality and compliance in the sterile drug manufacturing process. This individual will lead and oversee key quality operations functions, while ensuring alignment with customer & regulatory requirements and company objectives. The role requires a blend of technical expertise, analytical thinking, and leadership skills to address challenges, optimize processes, foster a culture of continuous improvement across the organization and enhance client relationships.</span></p></td></tr><tr><td valign=\"top\" style=\"width: 26.1474%; 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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Duties and Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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: 9.55px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#181818;'>Ensure compliance with cGMP, FDA, and other applicable regulatory requirements for sterile drug manufacturing.</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:#181818;'>Lead the team in quality oversight of manufacturing processes, ensuring adherence to SOPs and 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:#181818;'>Drive initiatives to strengthen aseptic technique, contamination control strategies, and data integrity practices.</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:#181818;'>Support the development and maintenance of a robust risk management program, ensuring all critical issues are addressed with sustainable solutions.</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:#181818;'>Serve as the quality operations representative during internal and external meetings with clients and other entities.</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:#181818;'>Respond to client inquiries, quality concerns, and requests in a timely and professional manner.</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:#181818;'>Oversee the resolution of client-related deviations, investigations, and CAPAs, ensuring timely closure.</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:#181818;'>Provide root cause analysis and implement preventive measures for recurring client concerns.</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:#181818;'>Lead cross-functional teams to ensure effective resolution of quality issues impacting clients.</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:#181818;'>Facilitate effective communication between clients and internal stakeholders to ensure alignment on quality objectives.</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:#181818;'>Travel</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#181818;'> </span><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#181818;'>as needed</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:#181818;'>Other duties as assigned</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 26.1474%; 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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Regulatory Responsibilities </span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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: 9.55px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#181818;'>Keep abreast of changes to qua</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#484848;'>l</span><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#181818;'>ity regulations and guidelines, advise the management team of any bus</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#484848;'>i</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#181818;'>ness </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#484848;'>i</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#181818;'>mplications of these changes</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:#181818;'>Maintain a deta</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#484848;'>il</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#181818;'>ed and comprehensive understanding of FDA, EU and other regulatory agency requ</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#484848;'>i</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#181818;'>rements</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:#181818;'>Conduct all work </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#484848;'>i</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#181818;'>n compliance with FDA, 21 CFR 820, 21 CFR 210 and 211 and other regulatory agency requirements</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 26.1474%; 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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Supervisory Responsibilities</span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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: 14.05px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#181818;'>Lead and direct work and provide feedback to a team of QA Specialists </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:#181818;'>Lead, manage and ensure proper training to any relevant change management programs throughout the company</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 26.1474%; 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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Experience</span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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: 14.05px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#161616;'>Eight to ten (8-10) </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'>years of progressively responsible related quality assurance experience</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 26.1474%; 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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Education</span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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: 14.05px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#161616;'>Bachelor's</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'> </span><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#161616;'>Degree</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 26.1474%; 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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;'>Knowledge, Skills & Abilities</span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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: 14.05px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#161616;'>Subject matter expertise </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#262626;'>in </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'>FDA, EU, and other 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:#161616;'>Comprehensive knowledge of QA concepts and principles</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:#161616;'>Knowledge of cGMP principles</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:#161616;'>Knowledge of RCA tools</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:#161616;'>Ability to work as part of a team</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:#161616;'>Management skills</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:#161616;'>Ability to manage multiple client relationships and priorities effectively</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:#161616;'>Good oral and written communication</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:#161616;'>Problem/situation analysis</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:#161616;'>Ability to build collaborative relationships</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:#161616;'>Uses good judgement</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:#161616;'>Perform complex work instructions and problem solving following established </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'>processes</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:#161616;'>Experience with Microsoft </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#030303;'>Office </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'>and general computer proficiency</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:#030303;'>Quality </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'>mindset and a willingness to develop yourself and others</span></li></ul></div></td></tr><tr><td valign=\"top\" style=\"width: 26.1474%; 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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><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:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><strong><span style='font-size:15px;font-family:\"Calibri\",sans-serif;color:#FF6600;'> </span></strong></p></td><td valign=\"top\" style=\"width: 73.8526%; 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: 14.05px;\"><li style='margin:0in;font-size:13px;font-family:\"Times New Roman\",serif;'><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#161616;'>Ability to remain stationary for long 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:#161616;'>Ability</span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'> </span><span style='font-family: \"Calibri\",sans-serif;font-size:15px;color:#161616;'>to move between locations</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:#161616;'>May occasionally lift up </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#262626;'>to </span><span style='font-family:\"Calibri\",sans-serif;font-size:15px;color:#161616;'>10 lbs.</span></li></ul></div></td></tr></tbody></table></div></div></div>\n",
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}Get this page with API
Rendered from the bluedoor Job Postings API. Reproduce it:
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