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Senior Quality Assurance Manager
Senior Quality Assurance ManagerAGSI • Santa Ana, CA, California, USA
Senior Quality Assurance Manager

Senior Quality Assurance Manager

AGSI • Santa Ana, CA, California, USA
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Job Title : Senior Quality Manager

Location : Orange County, CA

Salary : $130,000 - $155,000

We're looking for a Senior Quality Manager to oversee our Quality Systems, including the Quality Assurance and Technical Investigations Group (TIG). This is a high-impact role where you'll lead a talented team and champion initiatives that ensure excellence across every facet of our operations.

Just a snapshot of what you will manage :

  • Final product release
  • CAPA programs
  • QMS document control
  • Validations
  • Internal & external audits
  • Complaints & change notifications
  • Non-conformances

Key Responsibilities – Quality Leadership Role :

  • Lead and manage all aspects of the Quality Systems, ensuring compliance and continuous improvement.
  • Serve as a subject matter expert on quality regulations, including GMP and ISO standards.
  • Oversee and direct preparation for FDA and Notified Body inspections, acting as the primary quality liaison.
  • Coordinate and host internal and external audits, ensuring audit readiness and successful outcomes.
  • Drive and support product, process, and quality system improvement initiatives across the organization.
  • Deliver training and hands-on coaching on Quality System Regulations, ISO standards, and compliance best practices.
  • Develop and lead the Quality Systems team - including hiring, mentoring, performance management, and growth planning.
  • Monitor and analyze Quality Indicators and KPIs, providing actionable insights and leading effective CAPA strategies for ongoing improvement.
  • We're Looking For – Must-Have Qualifications :

  • Bachelor's Degree.
  • Auditor experience – at least 1 year preferred.
  • Hands-on experience in a regulated medical device manufacturing environment.
  • Solid understanding of U.S. and international medical device regulations, including : 21 CFR 820, 803, 804 (MDR), ISO 13485, ISO 14971, ISO 13408, EU MDR 2017 / 745 / MDD 93 / 42 / EEC, Canadian and Brazilian Medical Device Regulations.
  • Formal training in quality tools such as CQE, CQA, Six Sigma, Risk Assessment, FMEA, FTA, DOE, and Statistical Techniques.
  • Experience with validation of processes and equipment, method validations, process investigations, and technical evaluations.
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    Quality Assurance Manager • Santa Ana, CA, California, USA

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