Systems Test Engineer II — Medical Device (Onsite — Valencia,CA) Contract

Valencia, United States | Posted on 01/17/2026 From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at and follow us on LinkedIn: Job Description Our F500Medical Device client has an exciting opportunity for a Systems Test Engineer. Job Summary: Develops software systems, applications, firmware, and/or provides software systems testing and validation in support of R&D and/or Manufacturing Process Engineering. Responsible for analyzing, designing, programming, debugging, and modification of local, network/internet-related computer programs for commercial or end user applications (i.e. materials management, financial management, HRIS, or desktop applications products). May interface with users to define system requirements and/or necessary modifications. Responsible for developing, applying and maintaining quality standards for software products. Responsibilities Designs, develops, debugs, modifies, tests software programs by using current programming languages, methodologies and technologies. Documents software development and/or test development by writing documents, reports, memos, change requests. Methods used are determined by approved procedures and standards. Tracks software development effort by creating and maintaining records in the approved tracking management tool. Analyzes, evaluates, verifies requirements, software and systems by using software engineering practices. Investigates, researches, selects software designs, operating systems and/or practices. Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes. Quality Systems Duties and Responsibilities Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Minimum Qualifications 2-4 Years with BS (in Computer science or Electrical Engineering) 1-2 Years with MS Must have 4-5 years' experience in System Test verification, Python expertise, Github/Bitbucket experience Preferred Qualifications Medical Device industry experience Other Details Schedule: 08:00 AM - 04:30 PM Work Setup: Onsite in Valencia, CA Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment. #J-18808-Ljbffr Pharmavise Corporation