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 :
Location : Hyderabad, Telangana, India
Qualification required : M. Pharma/ MSc
Experience : M. pharma or MSc with 10+ years or 4+ years with PhD
Experience required with the LCMS, Isolation and characterization of Impurity, Experience in Preparative HPLC is required.
Candidate need to have good communication skills and technical skills.
Roles & Responsibility
Timely identify the requirements and responsible for Qualification of instruments / equipment’s (URS to Report) and periodic calibrations as per applicable site procedures.
Need to be a collaborating member with other teams to support project deliverables within agreed timelines, mentoring new joiners, active participation in project meetings / networks / meetings and contributing to Team goals while meeting individual objectives.
Candidate hired able to handle the design, plan and perform scientific experiments for projects at different clinical phases of drug substance and drug product with minimal guidance.
Personnel need to be well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports.
Should be able to perform investigations, guide team members, communicate proactively and clearly to global stakeholders.
Always required to adhere to Quality metrics, Compliance and Good Documentation Practices following ALCOA+ principles, GLP, OQM, HSE, ISEC and Novartis guidelines.