Senior Quality Engineer
$113,500–$125,000 year
On-site · Los Angeles, California, United States or Northridge, California, United States
Job Summary
Senior Quality Engineer to lead investigations, CAPAs and root-cause analysis within pharmaceutical/medical device manufacturing. Responsibilities include reviewing investigations, collaborating with stakeholders and customers, driving NPI activities, guiding Six Sigma-based quality improvement programs, supporting audits and regulatory inspections, and ensuring compliance across GMP documentation. Must effectively interact with customers, participate in inspection readiness, and provide guidance to quality improvement initiatives.
Required Qualifications
- Bachelor of science or engineering degree
- Minimum 5 years’ experience in pharmaceutical or medical device industry
- Ability to work independently with little or no guidance
- Experience with investigations, deviations, Non-conformances, CAPAs
- Experience in GMP documentation (SOPs, Protocols, Technical Reports) and regulatory inspections
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.