Quality Engineer - Med Device Job at Cypress HCM, Calabasas, CA

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  • Cypress HCM
  • Calabasas, CA

Job Description

The primary role of Manufacturing Quality function is to design, implement and monitoring quality control programs. Key deliverables include, but not limited to, recommending changes to methods, procedures and standards to improve quality of output based on analysis of data and systems. Ensures products are built correctly to specification, quality standards and appropriate regulatory compliance. Reports defects and tracks until resolution.

Responsibilities:

  • The primary objective of QA Engineering specialization within Manufacturing Quality Job Family is to design, implement and maintain quality assurance protocols and methods for processing materials into partially finished or finished products for supply chain.
  • Responsible for planning, implementing and managing compliance of in-house and outsourced manufacturing and production processes with internal and external quality and regulatory standards requirements for global distribution.
  • Reviewing methods and procedures for inspecting, testing and evaluating the precision and accuracy of production processes, production equipment and components, assemblies and/or finished products.
  • Performs analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.
  • Assures compliance to in-house and/or external specifications and standards (i.e.
  • MP, ISO, MDSAP).
  • Leads / facilitates investigations with cross functional team, to resolve and prevent recurrence of product and component issues in the supply chain by identifying appropriate root cause/s and corrective action/s.

Requirements:

  • Bachelor’s degree.
  • Minimum of 2 years of related experience Quality Engineering experience.
  • ISO 13485 knowledge

Pay Rate:

  • $35-48/hr

Job Tags

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