Please do not apply if you do not have all the experience mentioned in the below job description
Manage end-to-end supplier quality activities
Must be a certified Lead Auditor as per ISO 9001, or ISO 13485.
Assist in the QMS activities.
Good understanding of Medical and Pharmaceutical GMP/GLP/GDP practices.
Working knowledge of INV/CAPA, Change Control, and General Quality Systems process
Expertise in Internal Audits and CAPA closures.
Hands on experience in performing Supplier Audits and Supplier Qualification activities.
Good understanding on supplier performance monitoring and ensuring Supplier reliability.
Supporting for Quality metrics program.
Proficient experience with MS-office is required.
Responsible for identifying and performing gap analysis of Approved Supplier List
Strong written and verbal communication skills are essential
Experience working with virtual teams
Strong communication, teamwork, problem solving, decision-making, data analysis, inductive reasoning, critical thinking and root cause analysis skills are required.