Summary Reporting to the Asia Pacific Regional Complaints Centre (APRCC), Team Lead. This position is responsible for managing the activities and procedures associated with complaints in the Asia Pacific region. He/she is accountable for setting own work direction and completing work tasks which include the following- effective and timely processing of customer complaints including maintenance of complaint files, liaison with Business/ Customers/ Manufacturers, responses to customers and Complaint Quality reports; perform review of Adverse Events (injury complaints) for reportability to regulatory authorities.
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Why Join Us? A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you\xe2\x80\x99ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. Become a maker of possible with us!
Key Responsibilities
Review all Customer complaints about validity and assures complaints are processed in compliance with Company policies and procedures.
Responsible for all complaints originating in the region.
Implement and follow procedures to ensure timely and accurate receipt, logging, analysis, and response to customer complaints. These activities include:
Enter complaint information into the electronic complaint handling system. Generate acknowledgment emails. Complete Regional Decision Tree. Sample follow up/management. Assign complaint to Complaint Investigation Site (CIS) and/or Designated Complaint Handling Unit (DCHU) Monitor and update status. Generate customer response letters and coordinate translation (as needed). Closure of complaint in the system Complaint metrics tracking Complaint trend analysis and reports Notify and engage the manufacturing sites for investigation
Maintain systems to monitor and facilitate timely investigations and close out of open complaints. Ensure systems at workflow preclude lengthy unanswered complaints. Responsible for the management of the complaint handling process for the AP region, activities include:
Prepare and analyze complaint trends for the country/region. Monitor and communicate significant quality trends and identifying adequate corrective actions. Provide internal awareness of noted trends and quality issues via periodic and ad hoc reports.
Ensure the Customer complaint investigation, procedures, and activities comply with FDA Quality System Regulations, ISO, and Medical Device Directives for Vigilance.
Provide training to personnel involved in complaint investigation and complaint systems (such as Trackwise, Salesforce, Service-Max, etc) users, as a directive by the Supervisor.
Perform review of Adverse Events (injury complaints) for reportability to regulatory authorities for multiple countries according to BD procedures.
Exhibit flexibility and adaptability by managing assignments in accordance with project priorities and by altering the course of action when and where necessary.
Remain current in any upgrades to complaint handling systems.
Ensure that the Service Level Agreement (SLA) metrics are met.
Comply with all ISO 13485 requirements and BD policies.
Ensure a safe, healthy and environmentally friendly workplace by observing Company\xe2\x80\x99s rules and procedures. Active involvement in prevention, elimination of potential safety hazards and participation in activities which promotes recycling, replacement, and reduction of resource materials.
Executes any tasks and/or projects as assigned by the RCC Team Lead and/or Quality Manager, Greater Asia.
III. Education
Diploma or BS Degree desired, preferably in scientific, technical or engineering discipline, or applicable work experience
IV. Other Qualifications - Professional Certification/Key Licenses
Relevant quality assurance experience in quality systems for complaint management, failure investigation, corrective & preventive action, and document & quality records management.
V. Experience
Working experience in the pharmaceutical or medical device manufacturing industry is preferred.
VI. Required Knowledge and Skills
Working knowledge of Quality System standards and regulations ISO 9000:2008, ISO 13485: 2016 or US FDA QSR (21 CFR 803 & 820) will be an advantage.
Fluent in spoken and written English.
Good communication skills. Must be able to communicate precisely and accurately to all levels of the organization.
Continuous and versatile learning.
Drive for results and action oriented with a high sense of urgency.
Self-starter with the desire and ability to take initiative.
Demonstrated ability to work independently under time constraints, manage competing priorities and deadlines, and handle multiple tasks efficiently and effectively.
Must be able to identify and resolve problems and requests in a proactive and timely manner.
Must be able to gather and analyse information skilfully using problem-solving/root cause analysis skills.
Ability to exchange information clearly and concisely.
Ability to work for a large, fast-paced, matrix organization with speed and accuracy.
Ability to work well in a team-oriented environment.
Able to use Microsoft Excel spreadsheet with knowledge of formulas, statistical and modeling tools to identify and improve processes
Proficiency in statistical analysis and metrics reporting and associated tools and packages
Able to use PowerPoint skills for the creation/maintenance of organization charts and presentations.
Provide support to Customer Facing Teams
Click on apply if this sounds like you! Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
To learn more about BD visit: https://bd.com/careers
Primary Work Location MYS Kuala Lumpur - Jalan Kerinchi
Additional Locations
Work Shift MY2 Standard (Malaysia)
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