Job Summary:
This is a hybrid role with 3 days in office and 2 from home. As a key member of the supplier quality team, you will report to the senior quality engineer.
Key Responsibilities:
1. Lead/participate in continuous improvement activities.
2. Perform risk management activities in a cross-functional environment.
3. Evaluate documentation and work practices for compliance with ISO and regulatory requirements.
4. Develop and maintain the quality management system.
5. Assess the quality management system's effectiveness through internal audit and performance review.
6. Excel in interpersonal skills, working effectively in a team environment to meet targets and deadlines.
Required Qualifications: A third-level technical/science qualification plus at least 2 years' experience in the medical device/pharmaceutical industry, preferably in supplier management. Knowledge of quality management systems (ISO 13485, GMP).
Benefits: Competitive salary and benefits package.