Head of EMSO Quality

Job Description

External Manufacturing & Supply Operations Quality Management System on regional (Asia Pacific) level : Develops, Implements, maintains and continuously improves quality processes and systems to ensure the quality oversight of commercial products manufactured, packaged, tested and released at Contract Manufacturing Organizations (CMOs) EMSO Quality Oversight about CMOs : Implements, monitors, and reinforces Corporate Quality and TGO Standards at the CMO sites or suppliers, consistent with the business objectives, to ensure the manufacture of high quality pharmaceutical products, in accordance with regulatory compliance, internal, local, and international requirements to protect Tevas global branding. Supplier Evaluation, Due Diligence and Qualification : Collaborates with EMSO and Global Quality on the identification and spearheads the selection process of CMOs for third party projects EMSO Proactive CMO / Supplier Management : Establishes a closer collaboration with strategic CMOs /suppliers by adopting the key account management approach. (Supplier Relationship Management) Auditing of CMO : Ensure establishment and approval of the annual EMSO EU and APAC supplier audit plan Compliance issue : Ensures the GMP and regulatory compliance for EMSO products manufactured in the APAC Region for all TEVA markets Launches : Ensures Compliance with Pharmaceutical Regulations and TEVA Standards Budget: Establishes an annual regional budget for EMSO Quality as part of the AOP process, taking into account variable influences like volume changes, projects, launches, acquisitions and divestments, strategic and compliance remediation work.