Home › Companies › B52b0361 C892 47b8 A31d F03b13f6624e 19000101 000001 › Product Quality Engineer II
Product Quality Engineer II
B52b0361 C892 47b8 A31d F03b13f6624e 19000101 000001 · Wilmington, MA, US, Wilmington, MA · Active · ADP Workforce Now Recruiting
Job facts
| Field | Value |
|---|---|
| Company | B52b0361 C892 47b8 A31d F03b13f6624e 19000101 000001 |
| Title | Product Quality Engineer II |
| Normalized title | - |
| Department / team | - |
| Location | Wilmington, MA, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | ADP Workforce Now Recruiting |
| Posted / first seen | 2023-11-07 / 2026-05-31 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from B52b0361 C892 47b8 A31d F03b13f6624e 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 Wilmington. | 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 | B52b0361 C892 47b8 A31d F03b13f6624e 19000101 000001 |
| Source | b9ad03e6-b8f5-4e74-ad01-3a2e6bf4c3ab |
| ATS provider | ADP Workforce Now Recruiting |
Description
Job Summary:
The Product Quality Engineer II will be responsible for quality assurance activities including product quality engineering, non-conforming material report write ups and investigation, statistical process control, process improvements, and quality control oversight.
Essential Duties and Responsibilities:
Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the Quality department and work towards those goals. Prioritize and plan work activities; adapt for changing conditions. Assist in maintaining the quality system in accordance with applicable regulatory requirements. Identify quality system process improvements and implement solutions. Lead or assist with the Corrective Action/Preventive Action (CAPA) program. Lead or assist with the Customer Complaint system by performing complaint investigations, including root cause analysis. Assist with product inspections as needed. Perform Internal Quality Audits of the quality system Participate in supplier selection and approval process, including leading supplier audits and review of quality data. Perform investigations of non-conformances and drive corrective actions. Participate on cross-functional product development teams. Participate in product/process validations. Perform risk assessments, gathering cross-functional team input. Employ statistical techniques and rationale in decision-making activities driven to support non-conformance trending, CAPA effectiveness, part qualification, and process monitoring. Establish and trend quality metrics and data. Participate in third party audits against ISO 13485 and FDA 21 CFR Part 820 requirements. Other responsibilities as assigned.
Qualifications:
Bachelor of Science in Engineering, Science, or Biomedical. 2+ years of Quality Assurance/Quality Engineering experience in the medical device industry and/or experience in an FDA regulated environment is required. Knowledge of FDA 21 CFR Part 820 and ISO 13485, preferred. ASQ certification (Certified Quality Engineer, Certified Quality Auditor, Certified Biomedical Auditor) a plus.
Skills, Abilities, Competencies Required:
Excellent written and verbal communication skills. Able to work accurately in a fast-paced, hectic, ever-changing environment with strong attention to detail. Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness. Strong organizational, analytical, and time-management skills. Able to self-motivate and work both independently and as part of a team. Must have a solid knowledge of Microsoft office. Must be able to work in a team environment, execute responsibilities with minimal direct supervision, and have a high attention to detail. Demonstrated proficiency with FDA and ISO standards for Medical Devices.
restor3d is an Equal Opportunity Employer
Full job record
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| Source ID | b9ad03e6-b8f5-4e74-ad01-3a2e6bf4c3ab |
| Board ID | b9ad03e6-b8f5-4e74-ad01-3a2e6bf4c3ab |
| Provider | adp_workforcenow |
| Provider Job Key | 484165 |
| Title | Product Quality Engineer II |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Wilmington, MA, US, Wilmington, MA |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | MA |
| City | Wilmington |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=b52b0361-c892-47b8-a31d-f03b13f6624e&ccId=19000101_000001&lang=en_US&type=JS&jobId=484165&jwId=9200545382244_1 |
| Apply URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=b52b0361-c892-47b8-a31d-f03b13f6624e&ccId=19000101_000001&lang=en_US&type=JS&jobId=484165&jwId=9200545382244_1 |
| First Seen At | 2026-05-31 18:51:34Z |
| Last Seen At | 2026-06-06 12:42:04Z |
| Last Checked At | 2026-06-06 12:42:04Z |
| Last Changed At | 2026-06-06 12:42:04Z |
| Inactive At | — |
| Source Posted At | 2023-11-07 14:40:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=b52b0361-c892-47b8-a31d-f03b13f6624e|19000101_000001/date=2026-06-06/2026-06-06T12-41-13-347Z-843a109a341ec11d330467315ecd98d4d6493a5acabba2914fd158631877fcc5.json |
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