Test Engineer II

Actalent - Lafayette, CO

Full-time - Entry Level

Lafayette, CO

10,001+ employees

Administrative and Support Services

About the position

The Test Engineer II position at Actalent is responsible for developing strategies and performing verification and validation activities for software and systems in the medical device sector. This role requires technical expertise to solve complex problems and ensure that products meet quality and reliability standards. The engineer will work under limited direction and collaborate with various teams to support product development and compliance with safety and quality standards.

Responsibilities

• Plan, schedule, and manage the equipment required for testing, including exam, tool, fixture, and phantom design.
• Compile data and define changes required in test equipment, testing procedures, manufacturing processes, or new testing requirements.
• Frequently use and apply technical standards, principles, theories, concepts, and techniques.
• Responsible for verification and validation of new or changed products, including generating plans, protocols, and reports for testing performed.
• Create, develop, and maintain test software.
• Ensure test equipment is in good working order and calibrated as necessary.
• Coordinate and oversee the testing of equipment and product at outside test facilities.
• Set up and develop test tracking, monitoring, and data recording systems.
• Provide solutions to a variety of technical problems of varying scope and complexity.
• Participate in all phases of product development as needed, such as reviewing requirements, design, usability, risk assessment, and defects.
• Design, implement, and/or execute automated testing.
• Identify and implement process improvements.
• Participate in defect tracking and analysis.
• Troubleshoot, debug, maintain, and support existing products.
• Effectively communicate findings, problems, and solutions to project teams and stakeholders.
• Collaborate and maintain excellent working relationships with team members and stakeholders.
• Ensure all activities are performed in compliance with the Quality System.
• Perform duties in compliance with environmental health and safety-related site rules, policies, or governmental regulations.
• Perform all other duties as assigned.

Requirements

• Experience in a regulated environment (Aerospace, medical device, college labs, etc.)
• Experience with medical device verification and validation
• Working knowledge of software design, development, debug, and test practices
• Self-motivated with strong problem-solving skills and the ability to work independently
• Bachelor's degree in Engineering or Computer Science with a minimum of 2 years of experience or a Master's degree with 0 years of experience or a PhD with 0 years of experience.