Quality - Sr Quality Engineer

Viant Medical

Fremont (CA)

On-site

USD 120,000 - 170,000

Full time

14 days+
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Benefits offered by this job

Medical, dental, and vision benefits
Company-paid life insurance and DIS
Generous paid time off and holidays
401k Plan with Company Match
Tuition Reimbursement
Voluntary Universal Life and Long-Term

Job summary

Viant Medical in Fremont, CA seeks a Sr. Quality Engineer to lead quality activities across NCRs, complaints, CAPA and validation efforts. You will own quality subsystems, drive PFMEAs and control plans, and report metrics with cross‑functional teams.

Healthcare device experience is preferred and leadership of inspections is expected. You’ll collaborate on continuous improvement, supervise inspectors or technicians, and ensure compliance with QMS and regulatory standards, while maintaining

Qualifications

  • Bachelor's Degree or equivalent experience.
  • 7–10 years in Quality or related engineering roles within manufacturing environments.
  • Ability to lead root cause analysis with cross‑functional teams and drive corrective/preventive actions.
  • Experience in medical device manufacturing or similar plastics/chemicals environments.
  • Proficient with data analysis (Excel; Minitab preferred) to inform decisions and reports.
  • Experience producing validation reports and translating results into documentation.
  • Strong time management, proactive ownership, and adaptability to changing priorities.
  • Familiar with QMS and regulatory quality systems.

Responsibilities

  • Open, investigate, and close NCRs.
  • Open, investigate, and close complaints.
  • Create metric reports as assigned.
  • SPC monitoring and data-driven improvements.
  • Participate in CAPA projects and root cause analyses.
  • Participate in validation and measurement capability projects.
  • Update procedures as required.
  • Lead continuous improvement initiatives across the product line.
  • Own key quality subsystems and drive validations.
  • Create control plans and PFMEAs.
  • Perform internal audits and supplier qualifications.
  • Act as SME during regulatory inspections.
  • Lead Drumbeat customer meetings and report progress.

Skills

Root cause analysis
CAPA
Statistical analysis
Quality systems
Cross-functional leadership
Project management
Data analysis (Excel)
Validation reporting

Education

Bachelor's degree

Tools

Minitab
Microsoft Office

Job description

Quality - Sr. Quality Engineer

Job Responsibilities:

  • Open, investigate, and close NCRs.
  • Open, investigate, and close complaints.
  • Create metric reports as assigned.
  • SPC Monitoring
  • Participating in CAPA Projects
  • Participate in validation & measurement capability projects.
  • Update procedures as required.
  • Identify and perform continuous improvement projects.
  • Product line ownership
  • Execute validations.
  • Create control plans and PFMEAs.
  • Perform Internal Audit
  • Perform Supplier Qualification and audits.
  • Customer-facing role, running Drumbeat customer meetings.
  • Leadership role, direct reports of Inspectors or Technician
  • Owner of Critical Quality Subsystems
  • Act as SME in regulatory inspections.

Job Requirements:

  • Bachelor's Degree or equivalent experience
  • 7–10 years in Quality or related engineering roles within manufacturing environments
  • Ability to lead root cause analysis with cross‑functional teams and drive corrective/preventive actions.
  • Proficiency analyzing data (e.g., in Excel; exposure to Minitab preferred) to inform decisions and reports.
  • Direct experience producing validation reports and translating execution results into clear documentation.
  • Strong time/task management, responsiveness, proactive ownership, and ability to work with changing priorities.
  • Experience in medical device manufacturing; or other broader manufacturing such as plastics, chemicals, or polymer environments.
  • Proficient with math, statistics, and reading comprehension.
  • Proficient with computer skills (Microsoft Office, etc.)
  • Basic understanding of QMS
  • Solid understanding of Quality System Regulations (complaint, NCR, containment, root cause, etc.)
  • Functional Quality statistical knowledge (AQL, sampling, etc.)
  • Proficient with QMS
  • Strong leadership abilities
  • Capable of independent project management

Benefits:

  • New employees are eligible for the following benefits effective date of hire!
  • Medical, dental, and vision benefits
  • Company-paid life insurance and disability benefits
  • Generous Paid time off and 10 paid Holidays
  • 401k Plan with Company Match
  • Tuition Reimbursement
  • Voluntary Universal Life and Long-Term Care
  • Voluntary Legal Plan
  • Pet Insurance
  • Home Ownership Program
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