Quality System Engineer II

About Balt

Our purpose is to improve the lives of 150,000 patients in 2026.

Balt is a rapidly growing pioneer in an exceptional field. For 45 years, Balt has been leading the way - collaborating with physicians and institutions to develop elegant medical devices. Our products are being used by physicians across the world, and we have 13 offices in 11 countries – and counting.

We introduced one of the first neurovascular intervention devices in 1977 and now offer the world's broadest portfolio of medical devices for stroke. As the premier global neurovascular platform always seeking to expand beyond boundaries, we are now bringing our innovation to the peripheral vascular space.

We are proud of our mission, our people, and the incredible work we accomplish together as we empower physicians to save lives.

• Working at Balt means giving meaning to your work! Pride is a strong part of our identity.
• We are a close-knit team, with strong mission, vision and values that guide our day-to-day.
• Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.
• No matter the country, we take care of you.

Would you like to be part of our story? Don't hesitate, come and join us!

The Quality System Quality Engineer II will be responsible for supporting Balt USA’s quality system including, but not limited to, coordination of NCMRs and CAPAs, supporting audit execution, and supporting document control and training compliance.

This Quality Engineer will be expected to work directly with different functions while receiving support and guidance from other engineering staff and the QS Supervisor to complete tasks.

This position will have the responsibility to support and continuously improve current QS processes through technical and process innovation for the manufacture of neurovascular medical devices.

• Knowledge of quality systems for medical device manufacturing and requirements for manufacturing, inspection and testing.
• Plans, documents (protocol and reporting) product/process validations.
• Participate in audit activities.
• Initiate and/or verifies corrective and preventative actions resulting from NCMRs, CAPAs, audit findings and customer complaints.
• May help with qualifications for manufacturing transfer activities, including new or changed materials and processes, equipment IQ/OQ/PQ/PPQ.
• Identify, evaluate, and supports software validation activities.
• Lead meetings for process improvement and problem solving.
• Communicate with process stakeholders to address quality concerns and resolves issues.
• Maintain and develop processes and procedures by writing standard work instructions for quality system enhancements supporting production and quality controls.
• Have a clear understanding of FDA’s QMSR, ISO 13485 requirements, EU medical device regulation, and a good understanding in the application of statistics to process analysis and improvement.

• Bachelor’s degree required, preferably in an engineering or science discipline.
• 3+ years as an Engineer in a related field.
• Medical device or pharmaceutical experience.
• Data analysis skill set.
• ASQ certification a plus.

• Class II and III implantable medical device experience with focus on neurovascular devices.
• Strong communication skills working with multiple departments.
• A demonstrated ability to plan and run projects.

• Keen attention to detail when reviewing documentation and processes.
• Solid technical writing ability.
• Be able to work independently and cross functionally as part of a team.
• Comfortable communicating with a wide range of people from production, regulatory, management, suppliers, and other functions.
• General understanding of risk management, including design, use, and process FMEAs as well as a basic understanding of severity, occurrence, and risk mitigation and their impact on product and process controls.
• General understanding of process validation (OQ/PQ) and ability to develop test…