The opportunity
This role requires organization, management and control of the whole process of products transfer, but also for optimization and improvement of the technology on the already existing medical products on site. In addition, this role requires organization and control on the OPEX projects in the Production Site.
How you’ll spend your day
• Responsible for introduction of products and for transfers from R&D and other Teva sites or external contracted development labs
• Validates products to ensure commercial viability in accordance with regulatory requirements
• Leads the evaluation, remediation and optimization of products and processes, using statistical tools to ensure safety, quality, delivery and cost standards.
• Enhance productivity by exploring, analyzing, facilitating and leveraging efficiency initiatives for manufacturing processes
• Supports continuous improvement in MST processes, using Operational Excellence principles and relevant tools
• Leads site OPEX projects
• Ensures that changes to existing processes or the introduction of new processes are carried out and documented according to approved change control procedures and in compliance with cGMP requirements
• Works closely with R&D to provide input during formulation development and lead knowledge transfer from R&D to production regarding product, manufacturing process, and device for effective and efficient production
• Bridge the focus areas of R&D, Quality, EHS, Production, Supply Chain and Engineering to create common understanding and objectives and ensure robust products and flawless manufacturing
• Identifies recruits, develops and retains qualified MST professionals to provide technical support to the site
• Implements managerial practices to ensure a high performing MST team, modeling Teva values and leadership framework
• Brings global best practices into the site and actively shares site perspective, knowledge and lessons learned to contribute and support a best-in-class professional level of MST globally
