Quality Systems Engineer - Medical Device Manufacturing

The Quality Systems Engineer (QMS) - Medical Device Manufacturing will be responsible for the following;

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with ISO 13485 and FDA requirements.
• Manage internal audits and support external audits from regulatory bodies and customers.
• Ensure proper documentation control, including SOPs, work instructions, and quality records.
• Collaborate with cross-functional teams to address non-conformances and implement corrective/preventive actions (CAPA).
• Monitor and report on quality system performance metrics and drive continuous improvement.
• Support risk management activities and ensure compliance with applicable standards.
• Provide training and guidance on QMS processes to internal teams.
• Assist in new product introduction from a quality systems perspective.

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans, and all other qualified applicants.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.