Systems Engineer III

TALENT Software Services; Santa Clarita (CA); On-site; USD 120,000 - 160,000; Full time

Job summary

TALENT Software Services in Santa Clarita, CA seeks a software professional experienced in developing and validating software for medical devices and related systems. You will analyze requirements, design, develop, and test software, ensuring quality and regulatory readiness.

The role emphasizes system verification, statistical risk assessment, and strong cross-functional collaboration to deliver reliable software in a regulated environment. Hands-on coding and documentation are essential.

Qualifications

• BS in Computer Science or Engineering required; MS preferred.
• Python programming experience.
• Experience with test infrastructure verification and validation.
• Knowledge of system architecture and verification processes.
• Strong statistical analysis and risk assessment skills.
• Proven collaboration and communication abilities.

Responsibilities

• Designs, develops, debugs, modifies and tests software using current languages and standards.
• Documents software development and test activities with reports and change requests.
• Tracks development effort in approved project tracking tools.
• Analyzes and validates requirements and software against system needs.
• Researches and selects suitable software designs, OS, and practices.
• Continuously improves processes by coordinating with cross-functional teams.

Skills

Python

Test infrastructure

System architecture

System verification

Statistical analysis

Collaboration

Education

BS in CS/Engineering

MS in CS/Engineering

Job description

Job Purpose
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.

Description:
Job Purpose
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.

Key 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, research, 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.

Qualifications

Minimum 5 Years experience per below, with BS, 3 - 5 Years with MS

Must have:

• Python experience
• Test infrastructure verification and validation experience
• System architecture
• System verification
• Excellent statistical analysisRisk assessment experience
• Excellent collaboration and communications

Medical Device Experience Highly Preferred

Former regulated environment required