We now have an opportuntity for a highly motivated Quality Engineer to join our team. The Quality Engineer will provide support to manufacturing, helping to ensure delivery of highest quality product to the customer and to product development teams, helping to ensure development of highest quality new products.

Responsibilities

• Identifies and controls Manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria
• Develops Process Monitoring Systems by identifying critical process steps applying methods to reduce process variation in order to reduce/eliminate the cause of defects
• Leads process improvement efforts by identifying methods to capture quality metric data and by performing appropriate analysis methods to enhance sustaining product design and new product development
• Evaluates the adequacy and compliance of systems, operations, and practices against regulation and company documentation. Could serve as auditor of areas of the BSC quality system, such as development and manufacturing, as assigned
• Key partner in forming and evaluating the production area strategy for the production unit.
• Identify & lead quality projects to support Production Area Strategy.
• Quality lead on Production unit and quality process improvement projects.
• Lead on Preventive Quality initiatives in Production unit.
• Coordinates and conducts technical investigation and documentation of non-conforming events and trends, and develop technical investigation plans using Engineering Essentials.
• Leads investigations on customer internal & external complaints.
• Ensure Regulatory compliance in projects of responsibility by utilising quality tools and processes.
• Analyse preliminary plans and develop reliable engineering programs to achieve company, customer and governmental agency reliability objectives.
• Develop and/or review Process Qualifications, Test Method Validations, Gage R&R’s, Process Capability studies, Design of Experiment (DOE), production control plans.
• Leads process improvement efforts by performing appropriate analysis methods to enhance sustaining product design and new product development.
• Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
• Be part of a strong team culture around high expectations & high performance.
• Provide clear communication to stakeholders at key technical updates

What we can offer you:

• A Career with Meaningful Purpose – opportunity to transform the lives of patients worldwide
• Our Culture - our work is guided by core values that define our culture and empower our employees.
• Career Development – our highly engaged leaders will empower you to grow and will invest in your potential. You can also broaden your skills through personal development courses.
• Opportunity to Innovate – we encourage you to fulfil your true creative potential by speaking up with your ideas and solutions to problems that matter.
• Competitive Benefits – we offer market leading benefits including performance-related bonus, pension contribution and healthcare.
• Work-Life Balance – we have created a culture that acknowledges, respects and supports your life and work choices.
• Corporate Social Responsibility – we are dedicated to progressing business practices in areas important to our communities. Our onsite charity events have raised over €1.5 million for worthy causes in the past ten years.

Qualification Requirements:

• Higher Level Degree qualification in Engineering/Quality/Science with a minimum 5 years’ experience in a Medical Device environment or related industry.
• Demonstrate strong leadership skills, communication skills and promote quality at source.