
Associate Manager, Quality Complaints
- Marsa, Malta Island
- Permanent
- Full-time
- Provides leadership to the team members by providing problem resolution, process clarification, referrals to appropriate experts, and interpretation of Quality Management System procedures.
- Proactively prioritizes and balances utilization of resources to assure high quality investigations on 4000 complaints per month in a timely manner to meet Global Complaint Management KPIs.
- Interacts with management from Post Market Surveillance, Global Service Centers, R&D and External Contract Manufactures (ECM) to assure high quality and timely investigations.
- Escalates potential nonconformances and high risk complaints to Global Quality Management Representative (QMR).
- Responsible for development of product training programs and talent development of team. Successfully motivates the team for outstanding performance.
- Partners with Post Market Surveillance team to respond to complaint related inquiries from FDA / Global Ministries of Health.
- Identifies and manages continuous improvement projects with the objective of improving investigation quality and team productivity.
- Thorough knowledge of applicable procedures, specifications, regulations, and standards.
- Ability to manage a team of up to 10 employees.
- Strong analytical and problem-solving skills.
- Strong communication and leadership skills.
- Strong interpersonal/communication/influencing/negotiation skills
- Computer competency in Word, Excel, PowerPoint, and Minitab.
- Bachelor’s Degree in Engineering
- Minimum of 5 years of Medical Device experience in product complaints
- Minimum of 1-3 years manager experience preferred