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 | - |
| Salary | - |
| Status | active |
| ATS provider | ADP Workforce Now Recruiting |
| Posted / first seen | 2023-09-20 / 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/ Conformis is an Equal Opportunity Employer
Full job record
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| Board ID | b9ad03e6-b8f5-4e74-ad01-3a2e6bf4c3ab |
| Provider | adp_workforcenow |
| Provider Job Key | 480509 |
| Title | Product Quality Engineer II |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Wilmington, MA, US, Wilmington, MA |
| Department | — |
| Team | — |
| Employment Type | — |
| 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=480509&jwId=9200531886995_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=480509&jwId=9200531886995_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 | 2023-09-20 01:56:00Z |
| 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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