Tester

Title: Manual Test Engineer

Company: Medical Device Client [Details avail. via phone screen]

Work Model: 5 Days on Site (Lafayette, CO)

Engagement: 6 Month Contract (W2)

Rate: $35-$42/hr. (DOE)

As a Brooksource consultant working directly with our client, you will be a W2 employee with full-time 40 hour work week. Comprehensive benefits (health, vision, dental), paid holidays, & sick time accrual is available to all employees on contract.

About [Med. Device Client]

Together, we can change healthcare worldwide. We push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.

We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.

The Role

This position has the responsibility and authority to create and perform verification & validation activities for software and systems to ensure [client's] cutting-edge medical products meet our user’s needs and our quality and reliability standards. This position requires application of technical expertise to determine and develop approaches to solve complex technical problems with ingenuity and creativity. Work is performed under general direction.

Responsibilities

• Plan, schedule, and design test equipment, tools, and fixtures.
• Analyze data and define changes needed in test equipment, procedures, and processes.
• Apply technical standards and principles to testing activities.
• Verify and validate new or modified products, creating plans, protocols, and reports.
• Develop and maintain test software and ensure test equipment is calibrated and functional.
• Coordinate testing at external facilities and manage test tracking and data systems.
• Troubleshoot, analyze defects, implement process improvements, and communicate findings to teams.

Requirements

• BS/BA in Engineering or relevant degree
• Knowledge of applicable AAMI, ISO, FDA and EN standards
• Working knowledge of software design, development, debug and test practices.
• Extensive experience working in a regulatory environment
• Particularly experience with medical device testing and understanding of FDA Quality System Regulations (QSR)
• Oral and written communication skills.
• Ability to work in a team environment.

Nice to Have

• Able to handle multiple tasks/projects and manage priorities
• Experience with test automation including GUI, integration and stress testing and designing and implementing test automation frameworks.
• Project management skills including planning, estimation, tracking and communication
• Self-motivated with strong problem-solving skills and the ability to work independently
• Experience with Linux, Cypress, Selenium, JavaScript, C , Python, Perl, SQL, XML, continuous integration and other technical tools.
• Machine shop experience.
• Knowledge of statistical methods.

Eight Eleven Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, national origin, age, sex, citizenship, disability, genetic information, gender, sexual orientation, gender identity, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws.