About the role
With 64 manufacturing sites in 26 countries, our aspiration is to become the top manufacturer of innovative and generic medicines in the industry.
Position Purpose:
Operate equipment/s and execute assigned manufacturing tasks and activities according to production schedule to enable the timely production of products. Manage & overseeing compliance to all relevant cGMP documentation for the product being manufactured with the relevant GMP, safety and environmental guidelines. Perform routine operational support activities according the manufacturing process and schedule and enable the timely production of product with the quality and quantity an ensure that all activities and documentation comply with the requirement of safety, GDP/GMP, Data Integrity standards. Manage and oversee the modification, editing, distribution, review and archiving of GMP manufacturing documents and the edition of the Batch records in order to deliver them to Production in the quality and within the deadlines. Share knowledge and develop expertise of others and understanding of applied practice and processes in own area/discipline. Follow up to ensure production equipment to work properly with planned capacity in his/ her responsibility area. Ensure proper escalation of all matters related with HSE, quality, supply and production, implement decisions and act as responsible for continuity of production. Identify, assure and implement continuous improvement initiatives, which sustain Novartis competitive advantage. Actively participate collaborate with a trouble-shooting team to Ensure that the potential or actual process problems are correctly identified, and effectively resolved. Responsible for personal and professional development and support building organizational culture in line with Novartis values and behaviors.
Your key responsibilities:
Your responsibilities include, but are not limited to:
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