Regulatory Quality Engineer in Medical Devices

Become a Regulatory Quality Engineer at Medicom, where you will ensure compliance and quality standards in the medical device industry. This role provides a blend of hands-on and strategic responsibilities.
You will play a critical role in the development and documentation of the quality management system while supporting product development teams to meet regulatory requirements. Your expertise will help drive continuous improvement throughout the organization.

Key Responsibilities:

• Assist in developing a robust quality management system

• Collaborate on design and manufacturing quality assurance

• Manage supplier quality assessments and corrective actions

• Conduct internal audits and compliance checks

• Analyze quality data to support improvements
Requirements:

• Minimum of 3 years in quality systems for medical devices

• Bachelor's degree in Engineering or related field

• Comprehensive understanding of ISO standards

• Strong analytical skills for quality assessments

• Effective interpersonal skills for cross-team collaboration
Lead quality initiatives to uphold the highest standards at Medicom as a Regulatory Quality Engineer, ensuring product reliability and compliance.
#J-18808-Ljbffr