Home › Companies › 87a62329 A421 4ee6 Ae5c 12c4b6084d40 19000101 000001 › QA Specialist II, Supplier Quality
QA Specialist II, Supplier Quality
87a62329 A421 4ee6 Ae5c 12c4b6084d40 19000101 000001 · Hopkinton, MA, US, Hopkinton, MA · Active · $65,000–$80,000 / year · ADP Workforce Now Recruiting
Job facts
| Field | Value |
|---|---|
| Company | 87a62329 A421 4ee6 Ae5c 12c4b6084d40 19000101 000001 |
| Title | QA Specialist II, Supplier Quality |
| Normalized title | - |
| Department / team | - |
| Location | Hopkinton, MA, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | $65,000–$80,000 / year |
| Status | active |
| ATS provider | ADP Workforce Now Recruiting |
| Posted / first seen | 2026-05-22 / 2026-05-31 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from 87a62329 A421 4ee6 Ae5c 12c4b6084d40 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 Hopkinton. | 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 | 87a62329 A421 4ee6 Ae5c 12c4b6084d40 19000101 000001 |
| Source | f1aa2136-b65f-4e50-bba0-1f42439654a1 |
| ATS provider | ADP Workforce Now Recruiting |
Description
WHO WE ARE
RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.
THE ROSLINCT WAY
Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.
ACCELERATING YOUR FUTURE
The Quality Assurance Specialist II – Supplier Quality supports quality activities related to Supplier Quality Management in compliance with FDA regulations and internal SOP’s. Responsibilities include supplier documentation management, change management, performance monitoring, leading supplier-related corrective actions and investigations, and audit support.
How You Will Make an Impact:
Provide support the supplier qualification program by:
Onboarding new suppliers in support of new client programs Maintenance of supplier qualification documentation including questionnaires and quality agreements Support scheduling of audits and maintenance of the vendor audit schedule Support supplier audits and review of supplier response documentation Collaborate internally with key stakeholders in Supply Chain, Purchasing/Procurement, and Manufacturing Manage the Supplier Change Notification Program Review change notifications with cross-functional team and escalate customer and supplier notifications with potential impact Support change controls for raw material or supplier-related updates Monitor Supplier Corrective Action Request (SCAR) Program Maintain SCAR Log and initiate supplier corrective action activities resulting from deviations, non-conforming material reports, and/or supplier audits Follow up on action items to ensure completion What You Will Bring:
A highly organized work style that ensures timely execution of tasks. A mindset that ensures accurate results. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). Effective problem-solving capabilities. Strong oral and written communication skills. Qualifications:
B.S., in science, engineering, biochemistry, or related discipline, or combination of education, experience and training. Experience in cell therapy is a plus. 2-5 years with directly relevant experience in a regulated environment, biopharmaceutical environment or similar. Working knowledge of supplier quality, including supplier assessments/audits, maintaining supplier evaluation program, supplier corrective actions, and supplier process changes. Practical knowledge of US and EU cGMP regulations and guidance, GMP and GLP regulations. Past experience of participation in or leading internal or supplier audits Strong communication skills (written and verbal), influencing, negotiating and collaboration skills. Demonstrate strong organizational skills including ability to prioritize tasks and adhere to agreed timelines. Ability to manage and deliver multiple tasks with limited supervision. Travel may be required up to 10% of the time. OUR COMMITMENT
All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.
RoslinCT is proud to be an equal-opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.
Full job record
| Job ID | f634ad674882e5f85e12bbc6f4a0713bceef8596 |
| Org ID | 6ed0698a-e8fd-4e69-8e45-8b15c6ea142e |
| Source ID | f1aa2136-b65f-4e50-bba0-1f42439654a1 |
| Board ID | f1aa2136-b65f-4e50-bba0-1f42439654a1 |
| Provider | adp_workforcenow |
| Provider Job Key | 959695 |
| Title | QA Specialist II, Supplier Quality |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Hopkinton, MA, US, Hopkinton, MA |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | MA |
| City | Hopkinton |
| Salary Raw | 65000.00 To 80000.00 (USD) Annually |
| Salary Min | 65,000 |
| Salary Max | 80,000 |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=87a62329-a421-4ee6-ae5c-12c4b6084d40&ccId=19000101_000001&lang=en_US&type=JS&jobId=959695&jwId=9201537036343_1 |
| Apply URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=87a62329-a421-4ee6-ae5c-12c4b6084d40&ccId=19000101_000001&lang=en_US&type=JS&jobId=959695&jwId=9201537036343_1 |
| First Seen At | 2026-05-31 19:01:08Z |
| Last Seen At | 2026-06-06 12:47:13Z |
| Last Checked At | 2026-06-06 12:47:13Z |
| Last Changed At | 2026-06-06 12:47:13Z |
| Inactive At | — |
| Source Posted At | 2026-05-22 18:03:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=87a62329-a421-4ee6-ae5c-12c4b6084d40|19000101_000001/date=2026-06-06/2026-06-06T12-47-12-926Z-4fc9b7dcfbdbc357b8dd86b50ac3f4ac91da21eb989423d7a5c7bf86247a6d9d.json |
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"requisitionDescription": "<p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;' data-pasted=\"true\"><strong><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>WHO WE ARE </span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>RoslinCT is a world-leading cell and gene therapy contract development and manufacturing organization creating cutting-edge therapies that change people’s lives. Collaborative, dedicated, and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilizing ground-breaking science.</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><strong><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>THE ROSLINCT WAY </span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Here at RoslinCT, our team can contribute to the development of revolutionary treatments. We live every day by our core values: Partner Focus, One Team, Personal Growth, Integrity, Innovation, and Trust and Respect. We put our employees at the forefront by providing a flexible and empowering work environment, an attractive benefits package, and an emphasis on work-life balance. Our people are the key to our success. At RoslinCT we focus on developing our corporate culture, people’s development, growth, and the ability to impact patients.</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><strong><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>ACCELERATING YOUR FUTURE </span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style='font-family:\"Segoe UI\",sans-serif;'>The Quality Assurance Specialist II – Supplier Quality supports quality activities related to Supplier Quality Management in compliance with FDA regulations and internal SOP’s. Responsibilities include supplier documentation management, change management, performance monitoring, leading supplier-related corrective actions and investigations, and audit support. </span></p><p><strong><span style='font-size:16px;font-family:\"Segoe UI\",sans-serif;'> </span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:4.5pt;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong> </strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:4.5pt;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style='font-family:\"Segoe UI\",sans-serif;'>How You Will Make an Impact:</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:4.5pt;font-size:11.0pt;font-family:\"Times New Roman\",serif;'><span style='font-size:16px;line-height:107%;font-family:\"Segoe UI\",sans-serif;'>Provide support the supplier qualification program by:</span></p><div style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 39.5px;\"><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Onboarding new suppliers in support of new client programs</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Maintenance of supplier qualification documentation including questionnaires and quality agreements</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Support scheduling of audits and maintenance of the vendor audit schedule</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Support supplier audits and review of supplier response documentation</span></li></ul></div><div style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 35px;\"><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;'>Collaborate internally with key stakeholders in Supply Chain, Purchasing/Procurement, and Manufacturing </span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Manage the Supplier Change Notification Program </span><ul style=\"margin-bottom: 0in;list-style-type: circle;\"><li style=\"margin-top: 0in;margin-right: 0in;margin-bottom: 0.25in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Review change notifications with cross-functional team and escalate customer and supplier notifications with potential impact</span></li><li style=\"margin-top: 0in;margin-right: 0in;margin-bottom: 0.25in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Support change controls for raw material or supplier-related updates</span></li></ul></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Monitor Supplier Corrective Action Request (SCAR) Program</span><ul style=\"margin-bottom: 0in;list-style-type: circle;\"><li style=\"margin-top: 0in;margin-right: 0in;margin-bottom: 0.25in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Maintain SCAR Log and initiate supplier corrective action activities resulting from deviations, non-conforming material reports, and/or supplier audits</span></li><li style=\"margin-top: 0in;margin-right: 0in;margin-bottom: 0.25in;font-size:16px;font-family: initial;\"><span style='line-height:107%;font-family:\"Segoe UI\",sans-serif;font-size:16px;'>Follow up on action items to ensure completion</span></li></ul></li></ul></div><p style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style='font-family:\"Segoe UI\",sans-serif;'>What You Will Bring:</span></strong></p><ul type=\"disc\" style=\"margin-bottom:0in;\"><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;'>A highly organized work style that ensures timely execution of tasks.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;'>A mindset that ensures accurate results.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;'>Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;'>Effective problem-solving capabilities.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;'>Strong oral and written communication skills.</span></li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style='font-family:\"Segoe UI\",sans-serif;'>Qualifications:</span></strong></p><div style='margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: -0.25in;\"><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>B.S., in science, engineering, biochemistry, or related discipline, or combination of education, experience and training. Experience in cell therapy is a plus.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>2-5 years with directly relevant experience in a regulated environment, biopharmaceutical environment or similar.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Working knowledge of supplier quality, including supplier assessments/audits, maintaining supplier evaluation program, supplier corrective actions, and supplier process changes.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Practical knowledge of US and EU cGMP regulations and guidance, GMP and GLP regulations.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Past experience of participation in or leading internal or supplier audits</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Strong communication skills (written and verbal), influencing, negotiating and collaboration skills.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Demonstrate strong organizational skills including ability to prioritize tasks and adhere to agreed timelines.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Ability to manage and deliver multiple tasks with limited supervision.</span></li><li style=\"margin-top:0in;margin-right:0in;margin-bottom:.25in;margin-left:0in;font-size:16px;font-family: initial;\"><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>Travel may be required up to 10% of the time.</span></li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;' data-pasted=\"true\"><strong><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>OUR COMMITMENT</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways.</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:11.25pt;margin-left:0in;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><span style='font-family:\"Segoe UI\",sans-serif;color:black;'>RoslinCT is proud to be an equal-opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics.</span></p></div>\n",
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}Get this page with API
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GET https://api.bluedoor.sh/job-postings/v1/jobs/f634ad674882e5f85e12bbc6f4a0713bceef8596?include=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/6ed0698a-e8fd-4e69-8e45-8b15c6ea142eJSONGET https://api.bluedoor.sh/job-postings/v1/sources/f1aa2136-b65f-4e50-bba0-1f42439654a1JSONGET https://api.bluedoor.sh/job-postings/v1/jobs/f634ad674882e5f85e12bbc6f4a0713bceef8596/eventsJSON