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

Pharmavise Corporation
Posted 4 months ago, valid for 17 days
Location

Santa Clarita, CA, US

Salary

Competitive

Contract type

Contract

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Sonic Summary

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  • The job involves creating test methods and mentoring technicians in the investigation of product returns and non-returns.
  • Candidates must have a Bachelor's degree in Electrical Engineering and at least 4 years of relevant experience.
  • The position pays a competitive salary and requires proficiency in Microsoft Office tools and strong communication skills.
  • Responsibilities include leading engineering initiatives, coordinating failure investigations, and collaborating with various teams to determine root causes.
  • The role is onsite in Valencia, CA, with a contract length of 12 months, starting from May 25, 2026, to May 25, 2027, with the possibility of extension.

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 result 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. He/She will be responsible for creating monitoring IDs to assess the product performance and investigate performance changes using data analysis tools to find cause.

 

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







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