Unknown Company

Manager - Quality Assurance Engineering

irvine, california • Posted Yesterday
Remote Contract General


  • Ensures products meet customer requirements and complies with US and international regulations. Manages new product development and process improvement projects.

  • Hires, manages, trains, develops, reviews, and set goals for department and staff.

  • Acts as both coach and mentor to team members in areas of problem solving, decision-making, and process improvement.

  • Addresses all employee relations matters in a timely manner in coordination with Human Resources.

  • Manages and ensures staff’s adherence to Company policies and procedures.

  • Manages, modifies, and maintains a complete and comprehensive quality system to support development and contract manufacturing of medical products.

  • Oversees the technical side of the Company’s quality system and processes in relation to new product development and process improvement projects.

  • Oversees the implementation of new products against market and technical standards.

  • Evaluates the product manufacturing process and systems to ensure quality standards and timely and efficient flow of assigned projects.

  • Implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.

  • Participates in the reviewing of engineering designs to contribute quality requirements and considerations and supports areas in gathering and analyzing data.

  • Develops product/organizational quality assurance strategies including new European standards (MDSAP) where applicable.

  • Develops and analyzes reports related to department metrics. Prepares and presents organizational performance and technical information to the management team and associates.

  • Refines and implements quality product process plans and systems.

  • Develops and reviews standard operating procedures (SOPs) and other required policies.

  • Serves as quality engineering subject matter expert.

  • Serves as the quality representative on new product introduction teams.

  • Assures validation and compliance of contract manufacturing and sterilization facilities.

  • Manages Quality Engineering activities.

  • Organizes procedures and documentation related to areas of responsibility.

  • Participates in internal, external, and third party audits.

  • Provides technical assistance to other functional areas regarding interpretation of specifications, regulations, material qualifications, first article evaluations, and other quality related subjects to increase understanding of SOPs and guidance documentation.

  • Performs other related duties and projects as business needs require at direction of management.


Essential Functions



  • Ensures products meet customer requirements and complies with US and international regulations. Manages new product development and process improvement projects.

  • Hires, manages, trains, develops, reviews, and set goals for department and staff.

  • Acts as both coach and mentor to team members in areas of problem solving, decision-making, and process improvement.

  • Addresses all employee relations matters in a timely manner in coordination with Human Resources.

  • Manages and ensures staff’s adherence to Company policies and procedures.

  • Manages, modifies, and maintains a complete and comprehensive quality system to support development and contract manufacturing of medical products.

  • Oversees the technical side of the Company’s quality system and processes in relation to new product development and process improvement projects.

  • Oversees the implementation of new products against market and technical standards.

  • Evaluates the product manufacturing process and systems to ensure quality standards and timely and efficient flow of assigned projects.

  • Implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.

  • Participates in the reviewing of engineering designs to contribute quality requirements and considerations and supports areas in gathering and analyzing data.

  • Develops product/organizational quality assurance strategies including new European standards (MDSAP) where applicable.

  • Develops and analyzes reports related to department metrics. Prepares and presents organizational performance and technical information to the management team and associates.

  • Refines and implements quality product process plans and systems.

  • Develops and reviews standard operating procedures (SOPs) and other required policies.

  • Serves as quality engineering subject matter expert.

  • Serves as the quality representative on new product introduction teams.

  • Assures validation and compliance of contract manufacturing and sterilization facilities.

  • Manages Quality Engineering activities.

  • Organizes procedures and documentation related to areas of responsibility.

  • Participates in internal, external, and third party audits.

  • Provides technical assistance to other functional areas regarding interpretation of specifications, regulations, material qualifications, first article evaluations, and other quality related subjects to increase understanding of SOPs and guidance documentation.

  • Performs other related duties and projects as business needs require at direction of management.


Minimum Qualifications



  • Bachelor’s degree in a related engineering discipline.

  • Minimum seven (7) years of related quality assurance experience.

  • Previous management and leadership experience.

  • Advance knowledge with development and test requirements with recognized standards (ISO 13485).

  • Previous experience with New Product Development.

  • Demonstrated knowledge of the application of regulatory requirements for low-risk and high-risk software applications using a scalable approach.

  • Demonstrated knowledge and understanding on regulations and guidance as related to software development, SaMD.

  • Demonstrated ability to implement and improve Software QMS processes.

  • Previous quality assurance experience in materials manufacturing, preferred.


Pay range: $114,000 - 152,000/yr


Exact Compensation May Vary Based On Skills And Experience.


This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.

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