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 : Minimum of 6+ years of experience in Pharmaceutical production or QA or QC or Supply chain
Significant information on Public/Global pharma guidelines. Openness in executing and ceaselessly working on hearty quality frameworks and cycles, and keeping up with worldwide quality principles in managed regions.
Great information on risk-based approaches in item lifecycle the executives. Superb comprehension of business processes, store network standards and practices as well as supporting frameworks and applications
Great correspondence and relational abilities, Task the executives abilities and Change the board abilities.
Great application information (SAP, AQWA). Inside and out GxP information, Quality Gamble The executives, wide IT information, persistent improvement
Abilities to convey virtual and F2F Help phases of preparation. Give logical answers for guarantee consistence appropriate guidelines.
Experience of working intimately with the worldwide partners and exchange abilities
Job Roles and Responsibilities
• Openness in treatment of client protests and directing examination. Can freely deal with gatherings/conversation with colleagues/providers.
• Encounters in drafting of Value confirmation arrangement and Quality gamble evaluation for CMO's/providers. Grasping on Reviews and CAPA the board for providers. Solid grasping on Quality Administration Framework and GxP necessities.
• Openness of corporate capabilities and partner the board. Offer help in arrangement, audit and endorsement of GMP archives including nearby and worldwide SOPs, Wp's, Examination reports, and so on, where required.
• Guarantee execution of relevant Novartis QMS prerequisites at NTO GOC, QSC and CTS. Offer help as key client/Super client for IT apparatuses utilized for Quality Administration Framework.
• Support divisions in distinguishing holes/lacks in the laid out quality administration framework that can autonomously trigger, examine and execute the vital remedial activity in accordance with current outside and inner principles to guarantee nonstop development of the quality framework.
• Give opportune and successful correspondence of any potential consistence holes/takes a chance in QSC, NTO GOC and CTS to the separate SPOCs or group captain and work with for goal of recognized holes/gambles. Start, screen and satisfy the opportune survey of APQR reports for all the ESO centers/NTO that QSC upholds.
• Offer quality help to Nitrosamine risk based assessment/Changes, as required. Start and carry out quality improvement/disentanglement projects, at every possible opportunity. Confer preparation phases on GMP/Information respectability and other significant preparation stages, as required.
• Make different Kqi's/measurements for particular GxP exercises for both NTO GOC, QSC and CTS for introducing in significant gatherings. Offer quality help and endorsements in Guide item supply process. Guarantee all time availability of the exercises for inside/Colleague reviews (counting information uprightness reviews), have reviews, and oversee review activity plans for convenient conclusion of concurred CAPAs.
Walk-in for Freshers in Medo Pharm
Qualifcation : M. Pharma / B. Pharmacy
Division : Tablets and Capsules
Date of Walk-in : 29 Nov 22, time: 10-2 pm
Walk-in Venue : Medopharm Pvt. Ltd, Malur.. (Kolar DT ), No 34/B KIADB Industrial Area
Malur.. Via hosakote /Via Hosur