We're currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties Provides QA technical and compliance support for products and manufacturing related to suppliers, corrective and preventive actions, product/process improvements and training.Applies thorough, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.Plans, executes, reports and follows-up on quality system audits (supplier and internal).Actively participates in and supports departmental activities and responsibilities in accordance with existing procedures and external regulations.Makes decisions that are aligned with management objectives regarding work processes, plans and schedules to achieve quality objectives.Tracks and reports progress across projects and departmental commitments by reviewing schedules and due dates, identifying risks, and assisting teams with contingency plans.Resolves project issues by working with team members, management, suppliers, and others as appropriate.Assists department and project leaders in developing and reporting appropriate performance and quality metrics.Reviews and approves manufacturing, test and validation data/records to establish conformance to technical specifications and performance standards for existing, new or modified products and processes.Provides technical quality guidance to team members, technician and inspection staff. Education & Experience Bachelor's Degree in Engineering, Science or related technical field preferred.QA, Quality System or regulatory experience in the medical device or similar highly regulated manufacturing environment.
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