Job Summary:

Responsible for creating test methods, work instructions, training and mentoring technicians who work on investigation of return and not-return products. The QE will review result of investigations completed by others for accuracy, completeness and compliance to SOPs/WIs. The results of investigations can be used to escalate product issues in collaboration with other Post Market functions, R&D, Design Assurance, Operations, Supplier Management, and Medical Safety.

Responsibilities will include:

Understanding failure modes and approving product analysis for return and non-return complaints related to mechanical medical devices performed by technicians

Coordinating, training and supervising failure investigation activities for lab technicians

Support integration of new products into CIS lab by creating/validating test methods and test instructions

Creating and presenting slides for SER/CRB

Collaborating with other Post Market (CCC/CMC) teams, R&D, Design Assurance, Manufacturing, Supplier to help determine root cause of complaints

Monitoring product performance and escalating any non-conformance issues with returned device.

Creating, releasing new WI/SOPs in document control system

Initiating and owning non-conformance investigations

Training technicians to find root cause of complaints through sound failure analysis techniques

Minimum Qualifications:

Bachelor’s degree in Mechanical Engineering with 2+ years of relevant experience ***Bachelor's degree can be in electromechanical/electrical but the candidate needs to have hands-on experience in failure analysis.

Demonstrated problem-solving & failure analysis capabilities of mechanical systems/components

Proficient with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook

Great written/verbal communication skills and ability to collaborate with other teams

Ability to successfully multi-task and be adaptive

Preferred Qualifications:

Masters degree in Mechanical Engineering with at least 1 year experience in similar role

Ability to understand system level functionalities, to devise and validate test methods for failure analysis of systems/components

Experience in Medical Device industry

Familiarity with Post Market requirements and systems

Familiarity complaint systems used for medical devices

Experience with using SAP and PowerBI

Other Details:

Schedule: 08:00:AM - 04:30:PM

Work Setup: Onsite in Valencia, CA

Contract Length: 12 Months (5/25/2026 - 5/25/2027) and Possible Extension

Learn more about this Employer on their Career Site

Quality Engineer II — Medical Device (Onsite — Valencia, CA) Possible Contract Extension