Quality Engineer

Work Your Magic with us!  

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

Reporting to the Senior Quality Engineer, the Quality Engineer is responsible for managing the technical quality aspects for their respective areas working closely with the operations team to deliver on achieving all key department metrics.

• Responsible for all operational quality aspects associated with product manufacture and release.
• Responsible for the successful validation and qualification of process and raw material changes.
• Investigate Quality problems associated with the production department and implement effective corrective and preventive measures
• Support introduction of new products into the site ensure products are designed and validated to the required quality and regulatory standards.
• Ensures key quality metrics (CAPA management, First Pass Quality, Complaints, etc) are attained.
• Drive/support & implement continuous improvement projects with the operations team using Process Excellence lean/six sigma tools.
• Ensures the pertinent corporate quality and regulatory standards are attained.
• Maintains strong communication with internal and external stakeholders.
• Participates and supports the Internal and External Audit Programme.
• Apply G.M.P. and observe that it is being adhered to in the department.
• Participate in teams to help make necessary improvements and changes to all process related issues in the production department.
• Identify and Implement continuous improvements in conjunction with the operations team.
• Liaise with Vendors and Customers on quality related issues, internal and external.
• Supervises team of Quality Techs\ inspectors as required.
• Additional duties as required.

Requirements

Third level qualification or relevant knowledge and experience of Medical Device Directives; Previous experience in a similar role is desirable; Good investigative and problem-solving skills; Good Communication skills; Computer literate.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!