1. Ensure stringent Quality standards, norms & practices and effective deployment of GMP.
2. Develop & implement all manufacturing business systems covering all the functions.
3. Build and lead teams to achieve business goals.
4. Ensure OTIF manufacturing of Pharma & Oncology products as per the plan with the least cost in compliance with c GMP standards (USFDA).
5. Leverage human capital for improving their productivity; achieve operational excellence through sustained continuous improvement.
6. To ensure new products technology transfer and execution of batches as per agreed timelines
1. No critical observations in regulatory audits;
2. Establish benchmarks in manufacturing processes and related areas on a sustainable basis;
3. Be a good role model of a leader so as to inspire people in their own leadership development
4. Ensure a healthy work environment where people are motivated to work, learn and grow and not stressed.
This also means no politicization of environment will happen under his leadership
5. Zero Defect - Zero defects production, no quality Customer Complaints
6. Achieve set target top line & bottom-line, Block by Block, Line by line until 2015
7. Zero Slip - Tech. Transfer and Scale up of all the molecules in time. (Planning to Execution)
8. Zero Slip - OTIF – for all orders, outside as well as within India
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