We are looking for a remarkable Associate Quality Systems Specialist to join our incredible team at Medtronic Cardiac and Vascular in Taguig.
Growing your career as a Full Time Associate Quality Systems Specialist is a great opportunity to develop competitive skills.
If you are strong in leadership, planning and have the right initiative for the job, then apply for the position of Associate Quality Systems Specialist at Medtronic Cardiac and Vascular today!
Careers that Change Lives Bold thinking. Bolder actions. We are Medtronic.
Quality Assurance & Regulatory Affairs Shared Service Center team aims to be a strategic and trusted partner in Asia Pacific Region. Providing value-add services, drive reengineering of process, resource optimization and cost savings, we aspire excellence to drive solutions for centralized processes, integrate these values into what we do therefore enabling our stakeholders to achieve their goals with a balance of quality, productivity, cost, and effective service. A Day in the Life
The Associate Quality System Specialist PMV will ensure Post Market Vigilance are executed as defined in applicable quality documents. Responsible for assisting Quality Specialist on the execution, monitoring and closing of PMV throughout Southeast Asian regions. Responsible for assisting the implementation and maintenance of quality metric and monthly reports on PMV activities. Ensure that the Company's agreed quality standards (including ISO13485) are maintained with regards to products, procedures, policies, operations and customer contact Key Responsibilities: Support Asia Pacific Region Post Market Vigilance activities related to Product Complaint Handling Product Hold Order (PHO) Field Corrective Action Assist with the implementation and compliance to the company's Quality Management System. Analyze data to identify trends, opportunities for improvement and assist in the establishment of quality specifications and standards and support the development of processes and standards Assist with quality documentation, process mapping, reviewing processes and assisting with change initiatives Observe all health and safety policies and procedures and take all reasonable care that actions or omissions do not impact on the health and safety of others. Work within and actively promote Medtronic's Mission, corporate strategies, policies, procedures and Code of Conduct. Manage, update and track activities related to PMV-GCH timely and accurately Actively communicate and collaborate with PMV team and stakeholders and other duties as assigned by the Manager. Must Have Bachelor's degree required 0 years of experience required Your Profile: At least 2 years (Associate) or 3-4 years (Specialist) of quality experience in medical device industry or similar environment Good understanding of GDP and its implementation is required. Knowledge of ISO 13485 and its implementation will be an added advantage Complaint handling experience is an advantage. Knowledge in regulatory requirements for adverse event reporting for approved devices (FDA, TGA, MedSafe, HAS etc,) is a great advantage. Computer literacy including sound knowledge of the MS Office Suite or software Benefits of working as a Associate Quality Systems Specialist in Taguig:
? Learning opportunities
? Advancement opportunities
? Advantageous package
