Teva Site Quality Head - TAPI 

India, Madhya Pradesh, Gwalior 

263192495

• Lead the Quality organization, including Quality Control, Microbiology, Compliance, Systems, and Assurance Operations.
• Ensure and continuously improve the Quality Management System.
• Guarantee products meet cGMP requirements and registered specifications.
• Serve as the senior authority on product quality and market actions.
• Identify and mitigate quality risks to ensure product safety and effectiveness.
• Collaborate with Site GM and Global Quality to design and implement the site quality program.
• Oversee quality data management and delivery to stakeholders.
• Direct laboratory activities, including testing and approval of materials.
• Foster a culture of quality and encourage open communication and innovation.
• Maintain strong partnerships with the site leadership team.
• Act as a strategic partner to ensure project timelines and objectives are met.
• Provide leadership during inspections by internal, customer, and Health Authorities.
• Ensure Quality KPIs meet targets and monitor CAPA commitments.
• Manage the annual Quality Operations budget and resources.
• Assist the Head of Quality function TAPI and approve related documents.
• Perform additional responsibilities as assigned by the Head of Quality function TAPI

The ideal candidate will possess a degree in Chemistry, Science, Chemical Engineering, or a related scientific field. They should have over 10 years of experience in the pharmaceutical or API production industry, specifically in India. Proven experience in leading a Site Quality Head role.The candidate must have extensive experience in preparing for and managing inspections and audits from global authorities such as the FDA, local and European authorities, and Japanese regulatory bodies. They should have in-depth knowledge and hands-on experience in deviation management, Corrective and Preventive Actions (CAPA), quality systems, and handling complaints. Additionally, a solid background in Quality Control processes and practices is required.

Direct reporting line to Head of Quality with a dotted line to the Site General Manager.

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