Multiple openings in Novartis for QC Lead, Specialist - Quality & Clinical research associate

Multiple openings in Novartis for QC Lead, Specialist - Quality & Clinical research associate

 

Novartis Logo of 15th October 2021




About the Company : 


Novartis is 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.

About the job : 


Clinical Research associate :

Location : Mumbai

Minimum 2+ years in pharma with understanding of clinical trials and know the international standards like FDA, EMEA and ICH guidelines

it is required to travel up to 50% in this job role 


CRA job application


For Group Head QC : 

Job Location : Hyderabad

Qualification : Bachelors/Masters degree from a recognized university with health or management category. Should have a minimum of 10+ years of experience.


5+ years of minimum supervision is required.


View the job link 


Group head QC link


Associate Quality Operations : 

Location : Hyderabad 

Qualification : 3+ years 

Should have knowledge in Post marketing surveillance and ISO 13485.

Need to know about medical devices documentation

Should have knowledge on ISO 14971 Compliance guidance

Should review design history files 

Can apply from below 

Associate QA