Job Overview
This role requires experience and a proven track record in quality assurance and regulatory compliance of medical devices.
* Responsibility for adhering to policies, procedures, and relevant national and international regulations.
* Leading compliance and improvement initiatives associated with the quality system (e.g. corrective actions, audit programs, personnel training).
* Applying thorough, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues.
About this Role:
* Bachelor's degree in a related field such as engineering, life sciences, or business administration.
* At least 5 years of experience in quality assurance, quality management, or a related field.
* Proven ability to lead cross-functional teams and implement process improvements.
Benefits:
* A competitive salary and benefits package.
* The opportunity to work with a dynamic team and contribute to the success of our organization.
* Professional development opportunities to enhance your skills and knowledge.
What We Offer:
We are committed to providing a positive and inclusive work environment that supports the well-being of our employees.