
Resource Logistics
Reedsville, Pennsylvania • 13d ago
Easy Apply
Full-time, Third Party
$135,000 - $150,000
19 results (7 new)

Resource Logistics
Reedsville, Pennsylvania • 13d ago
Easy Apply
Full-time, Third Party
$135,000 - $150,000



Resource Logistics
Bedford, Massachusetts • Today
Easy Apply
Third Party, Contract
Depends on Experience











Job Title: Quality Manager - Medical Devices
Locations: Reedsville PA (Onsite) & Bothell WA (Onsite)
Job Type: Fulltime
Total Openings: 2
Salary: $130000 - $150000 per annum + Benefits
Job Description:
Lead quality remediation and compliance programs for medical devices, ensuring adherence to FDA, ISO 13485, and global regulatory requirements. Provide leadership for QMS processes, audit readiness, CAPA governance, quality metrics, and continuous improvement initiatives across cross-functional teams. |
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Reedsville, Pennsylvania
•
14d ago
Job Summary: Lead quality remediation and compliance programs for medical devices, ensuring adherence to FDA, ISO 13485, and global regulatory requirements. Provide leadership for QMS processes, audit readiness, CAPA governance, quality metrics, and continuous improvement initiatives across cross-functional teams. Key Responsibilities: Lead QMS, CAPA, Nonconformance, Complaint, and Audit programs.Support FDA inspections and regulatory audits.Drive quality remediation and compliance initiatives.M
Easy Apply
Contract, Third Party
Depends on Experience
Reedsville, Pennsylvania
•
12d ago
Role: Quality engineer / Lead/ Manager Medical Devices Manufacturing Experience Positions: 5 Openings Location: Reedsville, PA (Day 1 Onsite) Job Summary: Lead manufacturing quality assessment, remediation, and continuous improvement initiatives for Class II/ medical devices. Evaluate manufacturing processes, process validations, risk management activities, supplier quality systems, and compliance to FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, and MDSAP requirements. Drive yield
Easy Apply
Contract, Third Party
Depends on Experience
Reedsville, Pennsylvania
•
14d ago
Job Summary: Lead manufacturing quality assessment, remediation, and continuous improvement initiatives for Class II/ medical devices. Evaluate manufacturing processes, process validations, risk management activities, supplier quality systems, and compliance to FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, and MDSAP requirements. Drive yield improvement, CAPA effectiveness, quality metrics review, and manufacturing risk reduction programs across regulated manufacturing environments. Key Resp
Easy Apply
Third Party, Contract
55 - 60
No location provided
•
Today
Job Description Responsible for reviewing risk impact assessments and design change notifications received from R&D and Operations to evaluate potential impact to product safety, effectiveness, and the applicable risk management file. Apply risk management principles across R&D, Operations, and Post-Market Surveillance. Promote existing tools and proper utilization of the risk acceptability criteria. Facilitate cross-functional collaboration sessions with stakeholders from Manufacturing, Qualit
Full-time