Are you recruiting?
Advertise now

All Jobs in manufacturing/pharmaceutical

535 Matching Results

Senior Quality Engineer (Zimmer Biomet)

Zimmer Biomet
Posted :2 years ago

Planning Manager (Zimmer Biomet)

Zimmer Biomet
Posted :2 years ago

Quality Assurance Associate Director (Zimmer Biomet)

Zimmer Biomet
Posted :2 years ago

QC Analyst Level III(Viatris)

Viatris
Posted :2 years ago

Production Operative (Viatris)

Viatris
Posted :2 years ago

Production Operative – 3 Shift Rotating Cycle(Chanelle Pharma)

Posted :2 years ago
Zimmer Biomet

Zimmer Biomet

Senior Quality Engineer (Zimmer Biomet)

Posted :2 years ago
Job location
Galway, Ireland
Job type
Full time
Job Descriptions



Benefits:
  • Possibility to grow, develop, and be promoted within a Team
  • Friendly, warm and creative atmosphere
  • Healthy, inspiring, and international work environment
  • Ongoing coaching and talent development
  • Access to future career opportunities
  • Hybrid work model
  • Competitive reward packages
  • Annual bonus
  • Social and CSR events
  • Wellbeing initiatives

 

What You Can Expect

Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals.

How You Create Impact
  • Developing and implementing processes, procedures and instruction to sustain and improve the Quality Management System.
  • Supporting Top Management in the development and implementation of quality systems strategies and objectives.
  • Identifying and solving product and process problems
  • Supporting various operational /manufacturing groups and suppliers in resolving and preventing quality issues
  • Performing quality engineering analysis and responses for corrective/preventive actions
  • Working with suppliers, manufacturing, engineering, and other functional areas to assist and verify the implementation and effectiveness of the corrective/preventive actions taken for non-conformance.
  • Conducting audits and assessments of internal processes and suppliers manufacturing sites
  • Developing validation strategies and support the successful execution of same.
  • Supporting and representing the site during external regulatory audits.
What Will Make You Stand Out
  • Bachelor’s Degree in Quality or Engineering field, or an equivalent combination of education and experience.
  • Must be familiar with Microsoft Office Suite
  • Must have minimum of 5 years of experience in Quality Engineering field
  • Experience of working in a regulated industry, preferably medical devices.
What Will Make You Successful
  • Must be familiar with all aspects and elements of a quality system including but not limited to management responsibility, resource management, product realization and measurement, analysis and improvement processes.
  • Knowledge on aspects of quality assurance techniques such as: inspection methods, statistical sampling plans, gauging and test methods concepts, validation, and statistical process control
  • Demonstrated technical expertise
  • Demonstrates ownership for the integrity of work
  • Able to work independently or as part of a team and consider options for completing work
  • Strong written and verbal communication skills

Qualifications

Bachelors Degree in Engineering

Skills
  • Proficient in MS Office
  • Excellent written and verbal communication skills
Experience
  • 5+ years
1995