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 : 1-3 years in Pharma domain
Need to be a post graduate in Life science or pharmaceuticals
Strong knowledge in cGMP/ICH/QMS/GDP
Location : Mumbai
Job Role:
Oversees Quality perspectives and tasks inside area of obligation. - Guarantees and supports generally GxP similarity and Consistence with the Novartis Quality Administration Frameworks
Key Liabilities:
• Support the board of report based GMP consistence examination and Administrative consistence with the enlisted dossiers of Novartis Japan. Support Quality capable individual for Novartis Pharma Japan.
• Guarantee opportune assortment of required archives and data for report based GMP consistence assessment of assembling locales enlisted in Japan. Proficient correspondence with important partners and assembling destinations in opportune way.
• Support the accompanying administrative consistence action under GQP/QMS Work along with other line capabilities to keep the consistence of Japan endorsement records for the items. Powerful interchanges with assembling destinations.
• Change control connected with GMP consistence investigation. Support tasks of new sent off item and item move. GMP consistence investigation data. Assortment of required data and offer with pertinent partners, effective treatment of data and the board of basic data.
• Collaboration with Novartis Japan NCQ individuals. Status checking and pattern of archive assortment timetables. Report to Quality Confirmation Manager in Japan
• Audit gathered records and items checks. Guarantee that an ideal, successful, consistent quality improvement in substantiation with important partners. Satisfy the obligation of the Report The board and required Instruction and Preparing.