Senior Quality Systems Engineer role at Zimmer Biomet. Join a global medical technology leader improving mobility and enhancing life worldwide.
Responsibilities
Develop, implement, and continuously improve QMS processes, procedures, and instructions.
Act as SME for CAPA and Issue Evaluations, ensuring timely and effective closure.
Lead and maintain the internal audit program and support external audits of the site.
Host and manage regulatory inspections, including Notified Bodies (NBs) and FDA visits.
Support change management activities, preferably using Windchill or similar PLM systems.
Drive simplification of processes and implement innovative, technology-driven solutions, including AI-based tools for quality improvement.
Prepare and lead Quality Management Reviews to ensure QMS effectiveness.
Collaborate with operational/manufacturing groups and suppliers to resolve and prevent quality issues.
Provide training and coaching on QMS requirements to business users.
Qualifications
Strong knowledge of quality assurance techniques (inspection methods, statistical sampling, validation, SPC).
Expertise in CAPA, change management, and internal auditing.
Ability to apply innovative solutions and technology to optimize quality systems.
Excellent communication and leadership skills; ability to host regulators confidently.
Project management skills with ability to manage diverse tasks simultaneously.
Ability to work independently and make sound decisions.
Background
Bachelor’s degree in engineering or scientific discipline (or equivalent with CQE certification).
Minimum 5+ years of experience in Quality Systems, Quality Engineering, or Quality Compliance within a regulated industry (medical device preferred).
Experience with Windchill or similar PLM systems highly desirable.
Proven experience hosting regulatory inspections (NBs, FDA).
Familiarity with Microsoft Office Suite.
EOE/M/F/Vet/Disability. Location: Galway, County Galway, Ireland.
#J-18808-Ljbffr