Quality & Training Specialist
$72k - $80kClearPath Medical
About the job Quality & Training Specialist
About the Role
- Perform in-process and final inspections of medical cable assemblies to IPC/WHMA-A-620 and customer requirements
- Identify nonconformances, document findings, and initiate corrective action requests
- Conduct process audits to catch quality risks before they reach the customer
- Maintain inspection records, nonconformance reports, quality metrics, and calibration records
- Support internal, customer, and third-party audits
- Own the full NCR process: log, track, disposition, and close out nonconformances under Quality Manager guidance
- Initiate and coordinate CAPAs from root cause analysis through effectiveness verification
- Issue and follow up on supplier corrective action requests (SCARs)
- Communicate quality issues, containment actions, and resolution status to customers and suppliers via phone, email, and in person
- Develop and deliver training programs on IPC J-STD-001 and IPC/WHMA-A-620 standards
- Train new hires on assembly processes, quality expectations, and inspection techniques
- Serve as the in-house IPC subject matter expert and prepare operators for certification
- Maintain training records and certification status for all production staff
- Identify skills gaps and address them proactively with targeted instruction
- 3+ years in a manufacturing quality or production training role, preferably in medical device or contract manufacturing
- Hands-on experience with cable and wire harness assembly inspection
- Working knowledge of IPC J-STD-001 and IPC/WHMA-A-620 standards
- Ability to read engineering drawings, work instructions, and assembly documentation
- IPC J-STD-001 or IPC/WHMA-A-620 CIS or CIT certification (or commitment to obtain within 6 months)
- Experience managing nonconformances and CAPAs in a regulated environment
- High school diploma or equivalent required
- Associate or bachelor's degree in manufacturing, quality, or a related field
- Familiarity with ISO 13485 or FDA 21 CFR 820 quality systems
- Experience developing work instructions, training materials, or qualification checklists
- Take ownership and follow through without being micromanaged
- Communicate clearly and professionally with customers, suppliers, and teammates
- Have strong attention to detail and documentation discipline
- Can explain technical requirements to people at any skill level
- Approach problems with structure and see corrective actions through to resolution
- Salary: $72,000 - $80,000 per year, based on experience
- Employment Type: Full-Time
- Location: Tustin, CA
ClearPath Medical is an equal opportunity employer.
Vacancy posted 3 days ago
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