Openings in Novartis for Manager in Quality Operations

Openings in Novartis for Manager in Quality Operations

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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:

Job Location: Hyderabad

Qualification: Minimum of 8+ years required with Post graduation with sound knowledge in Pharma/QC/QA/ Synthetic chemistry.

Job Role:  

Oversight of all creation and testing exercises, guarantees consistence with cGxP, incl. information honesty and eCompliance - Backing exemption examinations - Survey and endorsement of creation, QC, and AS and T records - MBR audit - Backing OpEx improvement projects Qualified Individual - Executes cluster discharge in consistence with enrollment - Detailing of specialized objections/unfavorable occasions/extraordinary case situations connected with Novartis items in something like 24 hours of receipt - Dissemination of promoting tests (where relevant) Answerable for the assessment of substance amalgamation courses to distinguish, classify and control conceivable mutagenic debasements in dynamic drug fixings (Programming interface) and medication items Appraisal of potential corruption pathways of APIs in conclusive medication items with the reason to recognize and evaluate opportunities for the development of possibly mutagenic pollutions and ways of forestalling this. Take part in cross-utilitarian specialized groups as expected to follow through on projects. Engaged with paper-based appraisal of toxicological information for mutagenic, genotoxic and nitrosamines Direct of practicality reads up for conventional Programming interface amalgamation and union of results, corruption items and related substances. Security of protected innovation in the field of natural amalgamation. Use logical ability and compound data set to create answers for issues. Keeping up with research center logbooks and other task reports as per great documentation practice (information honesty) and HSE necessities. Co-appointment of research center work performed by professionals. Production of important directions, conventions and reports as per logical and administrative principles. Different undertakings as doled out by the manager and errands in view of a particular arrangement. Execution of and adherence to every one of the guidelines and necessities for safe work, climate security and property assurance. Obligation regarding individual and expert turn of events, ability