Sr. Quality Engineer

Sr. Quality Engineer

Contract Type:

Contractor

Location:

Irvine

Industry:

Pharmaceuticals

Contact Name:

Flora Pollack

Contact Phone:

Date Published:

06-Jan-2026

Sr. Quality Engineer

Irvine, CA

Schedule: Standard Office Hours

Duration: 18-Month Contract

Pay:$51-56/hr (W2)




Our client is a leading global medical technology company specializing in innovative healthcare solutions. They are seeking a Sr. Quality Engineer to support R&D and Operations teams in design engineering, risk management, and regulatory compliance activities.




Essential Functions and Responsibilities

  • Collaborate with R&D and Operations teams in the areas of Design Engineering, Risk Management, Design Controls, Design Verification, Statistical Techniques, Test Method Development, Process Development, Quality Assurance, and Regulatory Compliance
  • Investigate moderately complex manufacturing product quality for all production processes based on engineering principles, analyze results, and make recommendations
  • Identify and ensure the optimization of complex Manufacturing and/or R&D processes using engineering methods for design for manufacturing and for continuous process improvement
  • Identify opportunities for re-design/design of basic equipment, tools, fixtures, etc. to improve manufacturing processes and reduce risk
  • Lead Risk Management process for project in compliance to appropriate external standards and corporate policies, to ensure critical to quality features are identified and addressed appropriately
  • Create and maintain risk management documentation such as risk management worksheet and FMEAs in alignment with ISO:14971
  • Provide integral technical input for the development of project plans, project timelines and strategy to support premarket approval of products
  • Partner with R&D engineers to support design verification/validation strategy and testing, including test method development/validation activities
  • Mentor engineers in understanding of quality systems and strategies within new product development
  • Support root cause investigations/product evaluations for product failures encountered during clinical use using engineering methods (Six Sigma, DMAIC, etc.)
  • Support resolution of manufacturing and compliance issues (i.e. CAPA, non-conformances, audit observations, etc.) utilizing problem solving tools
  • Support Quality Engineering activities to improve customer satisfaction and successful achievement of company quality objectives
  • Ensure compliance with all National/Federal, local, and company regulations, policies and procedures
  • Train, coach, and guide lower-level employees on more complex procedures
  • Oversee Quality support tasks, give instruction to engineers/technicians on conducting tests, train engineers/technicians and provide feedback, and may coordinate engineers/technician work

Education and Experience

  • Bachelor's degree in engineering required
  • 5-7 years experience required

Knowledge and Skills

  • Basic leadership and mentoring skills necessary to provide support and constructive performance feedback
  • Ability to read and interpret blueprints, technical drawing, schematics and computer-generated reports
  • Previous experience with computer applications and software related to engineering field, such as Computer Aided Design (CAD)

...

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