About Your New Job Join a leading global pharmaceutical company with a strong reputation for innovation and excellence.
This is your opportunity to work on cutting-edge products in a collaborative and dynamic environment.
This is a 12-month contract based in Co. Mayo.
As a Complaints Processing Analyst, you will play a crucial role in ensuring customer complaints are handled efficiently and in compliance with global regulations.
Reporting to the Complaints Manager, you will oversee investigations, identify root causes, and track corrective/preventive actions to resolution.
Your responsibilities as a Quality Complaints Analyst Ensure all complaint records meet global regulatory requirements.Investigate and document product complaints, including root cause analysis and CAPA implementation.Coordinate cross-functional activities related to adverse events, product quality concerns, and customer service complaints.Work closely with internal departments to drive timely complaint resolution.Serve as a subject matter expert on complaint handling and compliance.What Skills You Need as a Quality Complaints Analyst Bachelor's degree in Sciences or a related field.1-2 years of experience in the pharmaceutical industry.Knowledge of global regulatory requirements for pharmaceuticals, medical devices, and combination products.2 years of GMP experience.Strong technical writing, analytical, and problem-solving skills.Proficiency in SAP, TrackWise, and document management systems (desirable).Excellent communication, organizational, and time management skills.What's on Offer Competitive hourly rate.Experience working in a leading pharmaceutical company.Ongoing training and career development opportunities.Be part of a collaborative team in a global pharmaceutical leader.What's Next?
Apply now by clicking the "Apply Now" button or call Elaine McCarthy at +353 21 4847135 for more details.
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