What are the responsibilities and job description for the Quality Engineer III — Medical Device (Onsite — Valencia, CA) Possible Contract Extension position at Pharmavise Corporation?
Job Summary:
Responsibilities will include:
Providing leadership role on championing departmental or cross-functional engineering initiatives
Understanding failure modes and approving product analysis for return and non-return complaints related to electro-mechanical 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 devices
Creating and maintaining of product performance trends based on UPN and code groupings.
Investigating trend excursions by doing data analysis to find cause
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 Electrical Engineering with 4 years of relevant experience
Demonstrated problem-solving & failure analysis capabilities of electronics systems/components including those with RF communication
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
Understanding of RF communication scheme/concepts
Requires working in San Diego for a few months
Preferred Qualifications:
Masters degree in Electrical Engineering with 2-3 years 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
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