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Business Unit Overview:

This position is part of Novanta Medical GmbH business unit. Specialized in the field of Minimally Invasive Medicine, WOM develops devices and accessories so that doctors can operate with small cuts. We produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. Our insufflators and pump systems dilate cavities in the body and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate.

Job Summary:

As a Junior Test and Verification Engineer, you will support the testing and verification of the quality and compliance of medical devices and tubing sets. Working closely with experienced engineers, your role involves preparing and executing test cases and test runs, building and validating test stations, documenting results, and collaborating with cross-functional teams. This is an excellent opportunity to develop your skills in a regulated medical device environment while contributing to product quality, safety, and adherence to industry standards.

We are looking for a motivated Junior Test and Verification Engineer to join our team and grow into a key contributor to the reliability and effectiveness of our medical devices.

Primary Responsibilities

Support the Test Strategy: Contribute to the implementation of a cross-device, unified test strategy in line with the guidelines of the architecture group, while learning the team’s testing processes and methods.

• Develop and Execute Test Specifications for System Tests: Prepare test specifications for system tests under the guidance of experienced engineers, review the testability of the designed test cases and procedures for both software and hardware systems, align them with product requirements, and execute them according to the test plan.
• Execute and Document System and Component Tests: Carry out and document system and component tests (Level 2 and Level 3) according to the test plan, recording results accurately and completely.
• Prototype and Functional Sample Support: Participate in the building of functional samples and prototypes, conduct tests to validate design concepts, and provide feedback to the engineering team.
• Documentation Control: Maintain and control documents related to testing procedures, protocols, and reports to ensure version control and traceability.
• Conduct Functional, Performance, and Regression Testing: Perform various types of testing, including functional, performance, and regression testing, to ensure that the system meets specified requirements and quality standards.
• Utilize Testing Equipment and Tools: Use the required testing equipment and tools to conduct tests and accurately interpret test results.
• Identify, Document, and Track Defects and Issues: Identify, document, and track defects and issues discovered during testing, providing detailed records for resolution and supporting root cause analysis.
• Build Device and Component Test Stations: Support the development of device and component test stations for medical production and development, including creating hardware and software concepts (incl. sensor technology) and implementing them.
• Verify and Validate Test Stations: Conduct verifications and validations of inspection and test stations to ensure they operate reliably and produce accurate results.
• Maintain Device and Test Equipment Lists: Create and maintain device lists and lists of test equipment to support traceability and availability.
• Test Execution: Conduct various tests and experiments, which may involve performance testing, electrical testing, pressure testing, and other relevant evaluations. Ensure that the tests are conducted according to the established protocols.
• Data Collection and Analysis: Record test data accurately and comprehensively. Analyze the results to identify deviations, anomalies, or areas that may need improvement. Document any issues or defects discovered during testing.
• Calibration and Maintenance: Ensure that testing equipment is properly calibrated and maintained to provide accurate and reliable results. Perform routine maintenance and calibration checks on testing instruments.
• Adhere to Testing Deadlines: Conduct testing and validation activities according to any required deadlines, ensuring that testing milestones are met.
• Compliance with Policies: Strictly observe all policies within the test rooms, laboratories, and offices, ensuring a safe and compliant work environment.
• Cross-Functional Collaboration: Collaborate with various teams, including design engineers, production teams, and quality assurance personnel to ensure that the product meets design specifications and quality standards.

Requirements:

• Education and Training: A bachelor’s degree (or equivalent) in a relevant field, such as electrical engineering, biomedical engineering, mechatronics, or a related technical discipline. Recent graduates and candidates completing their studies are encouraged to apply.
• Relevant Experience: This is an entry-level position; little to no professional experience is required. Internships, working-student roles, academic projects, or a thesis in testing, quality assurance, electronics, or software development is an advantage. A willingness to learn and grow within a regulated medical device environment is essential.
• Knowledge of Regulatory Compliance: A basic awareness of, or an interest in learning, medical device regulatory standards such as ISO 13485 and FDA regulations. Exposure to regulated industries or quality management systems (QMS) is a plus but not required.
• Testing and Verification Skills: A foundational understanding of test execution and test case design, with a keen interest in developing skills in test planning and in functional, performance, and regression testing.
• Strong analytical and problem-solving skills, with the ability to help identify defects and issues and to support root cause analysis.
• Test Automation: Basic programming or scripting knowledge (e.g., Python, C#, or a similar language) and an interest in test automation is an advantage.
• Quality Assurance and Compliance: A solid understanding of quality assurance principles and a willingness to learn the regulatory standards specific to medical devices.
• Strong documentation skills for creating and maintaining test plans, test cases, and test reports. Attention to detail is essential to ensure accurate record-keeping.
• Equipment and Tool Proficiency: A willingness to learn to use testing equipment and tools relevant to the medical device industry and to interpret test results accurately.
• Excellent teamwork and communication skills to work effectively with cross-functional teams, including engineers, quality assurance personnel, and production teams.
• Attention to Detail: Meticulous attention to detail to identify deviations and ensure product specifications are met.
• Time Management: Effective time management to meet testing deadlines and ensure products are validated on schedule.
• Safety Awareness: Strict adherence to safety protocols, especially when working with medical devices, to maintain a safe working environment.

Travel Requirements

• none

Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy.

Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.