QC Supervisor: Global Medical Device Quality Lead

Vitalograph; Ennis; On-site; EUR 55,000 - 75,000; Full time

Benefits offered by this job

Pension plan

Health insurance

Education assistance

Job summary

Vitalograph in Ireland is seeking a QC Supervisor to lead day-to-day QC inspection activities in a regulated medical device environment. You will coordinate inspection plans, manage a team of QC Inspectors, and ensure compliance with ISO 13485 while driving continuous improvement.

The ideal candidate has a BSc in science or engineering, at least 2 years in medical device QA, 2 years of leadership, and strong MS Office skills, with excellent communication and metric analysis capabilities.

Qualifications

• Minimum of a BSc in a Science or Engineering discipline.
• At least 2 years' experience in medical device manufacturing within a QA role, using ISO 13485.
• At least 2 years' leadership/people management experience.
• Excellent skills with Microsoft Word, Excel and other Microsoft Office packages.
• Strong communication skills, coupled with diligence in metric analysis.

Responsibilities

• Coordinate and prepare weekly inspection plans.
• Ensure all work and tasks carried out are consistent with and compliant with our QA systems.
• Monitor QC Inspector work throughput and measure individual work throughput on a daily/weekly basis.
• Manage timekeeping and clock-card maintenance for QC Inspectors.
• Coordinate and analyse inspection resource requirements to best fulfil both long-term and immediate production order requirements.
• Participate in wider team meetings to support fulfilment of the company’s sales order plan.
• Manage QC NC/CAPA activities and participate in root cause analysis, identification and resolution.
• Assist with and participate in internal and supplier audits.
• Draft SOPs and associated documentation for the QMS.
• Complete timely record and metric-related transactions.
• Complete regular metrics and data reporting for management.
• Contribute to Continuous Improvement initiatives.
• Perform other duties as may be assigned in support of compliance or QMS activities.
• Ability to travel overseas as part of the role is required.

Skills

Leadership

Quality Assurance

Regulatory Knowledge

Education

BSc in Science or Engineering

Tools

MS Word

MS Excel

QA Software

Job description

Vitalograph in Ireland is seeking a QC Supervisor to lead day-to-day QC inspection activities in a regulated medical device environment. You will coordinate inspection plans, manage a team of QC Inspectors, and ensure compliance with ISO 13485 while driving continuous improvement.

The ideal candidate has a BSc in science or engineering, at least 2 years in medical device QA, 2 years of leadership, and strong MS Office skills, with excellent communication and metric analysis capabilities.