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 ofR&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 userapplications (i.e. materials management, financial management, HRIS, or desktopapplications products). May interface with users to define system requirementsand/or necessary modifications. Responsible for developing, applying andmaintaining quality standards for software products.

Responsibilities:

- 1. Designs, develops, debugs, modifies, tests software programs by usingcurrent programming languages, methodologies and technologies.
- 2. Documents software development and/ortest development by writing documents,



reports, memos, change requests. Methodsused are determined by approved procedures and standards.

- 3. Tracks software development effort bycreating and maintaining records in the approved tracking management tool.

- 4. Analyzes, evaluates, verifiesrequirements, software and systems by using software engineering practices.

- 5. Investigates, research, selectssoftware designs, operating systems and/or practices.

- 6. Continuously improves process andwork methodologies by interfacing with peers/cross-functional groups andanalyzing activities to improve workflow and work processes.

Quality Systems Duties andResponsibilities:

Build Quality into all aspects of theirwork by maintaining compliance to all quality requirements.

Minimum Qualifications

- 2- 4 Years with BS (in Computer science or Electrical Engineering) 1 - 2 Yearswith MS
- Musthave 4-5 years' experience in System Test verification, Python expertise,Github/Bitbucket exp

Preferred Qualifications

- MedicalDevice 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.

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📌 Systems Test Engineer II — Medical Device (Onsite — Valencia,CA) Contract
🏢 Pharmavise
📍 Valencia