At the forefront of innovation, a Quality Engineer II drives transformative change within the medical device industry.
This pivotal role requires unwavering dedication to quality practices, ensuring seamless compliance with regulatory standards. By embracing problem-solving and driving process improvements, you will be instrumental in propelling our organization forward.
This position involves:
* Developing and implementing quality procedures that foster an environment of excellence;
* Collaborating with cross-functional teams to drive impactful process enhancements;
* Conducting thorough risk assessments and providing actionable recommendations for corrective actions;
* Maintaining meticulous records and documentation;
As a key player in this endeavor, you will possess a Level 8 degree in a relevant field such as Mechanical Engineering, Biomedical Engineering or a related discipline. With at least 3-4 years of engineering experience in a regulated environment, preferably medical devices, you will bring invaluable expertise to our team.