About Novartis
One of the largest pharmaceutical company of swiss origin located in Basel, Switzerland. Originated by merging of Ceiba and Geigy in 1996.The company further classified its operations to 3 major divisions: Sandoz (generics), Alcon (eyecare) and innovative medicines, it has 33.3% ,24.9% of the Roche shares and identic pharma respectively. The firm established its Multi functional center in Hyderabad, which covers of around 870,000 Square feet.
The pharma giant has a large portfolio of medicines in treating areas including but not limited to osteoporosis, Psoriasis, COPD, Hypertension, Alzheimer’s disease, heart failure, malaria, Amoebiasis, Asthma, schizophrenia and so on. This laid its step in animal health division, pests and rodent control by providing many varieties of products like milbemax, interceptor, Acara.
United states department of Health and human services in the year 2009, awarded Novartis with $ 486 contract for producing cell based influenza vaccine with a motto of 150,000,000 doses of flu pandemic vaccines with in 6 months. When gone through the financial aspect, it has a revenue of $ 53 billion and market capitalization of over $ 209 billion.
Recently decoding the hand of Artificial intelligence around pathological cancer, by recognizing the cancer at various stages. The firm has huge corporate responsibility helping in addressing the needs of undeserved populations, 24 Million patients reached access through the programs in 2018 and over 17 Million people reached training, health education services.
About the Job
Experience : 12+ years of experience in Pharma or supply management or clinical management. Required experience in IT systems as systems admin and handling of URS
Need to have sound knowledge in Production, QA, Technical development and regulatory knowledge.
Should have good organizational and decision making skills and need to have cGMP compliance understanding
Required to support and provide service within the teams of associates and maintain regulatory files handling inspections and assist with the authority management.
required to manage and handle activities like quality plan initiatives that is about quality objectives to assure compliance with GXP regulations
required to support project team members and provide GMP related topics support and comply with internal and external guidelines regarding safety and quality.
maintain and improve the quality performance and compliance including risk management reporting health authority and it systems
able to preview decide and approve as well as release of GMP related deliverables and related tools as per the responsibility in order to ensure the compliance with CGMP and project quality deliverables
able to manage internal and external auditor auditor and follow the respective guidelines manage portfolio development and new tools improve the quality initiatives and quality management implementation and training activities