About Pfizer
One of the major contributor of medicines globally ranking in top 10 pharma companies. The industry equipped with more than 1500 scientists with more than 5 million testing labs globally and over 36 clinical trials before the first perception. In the area of biotechnological medicine with 25000 clinical researchers testing every day world wide.
The company has located its head quarters in New York with the rank 57 in fortune 500 companies, founded in 1849, which is 170 years ago. Form have joint ventures with GSK and Mylan for improving the quality of medicines.
Large portfolio including branded and generics with products listed from A to Z. Applies rare diseases research to unveil the new therapy treatment, more than 30 million people in USA and 350 million globally uses the medicines for rare disease treatments. Several hematological and neurological rare disease therapies are in research phase. Gene therapy is one of the promising and rapidly developing portfolio in the companies profile, placing genetically corrected copies to patients cells. Having collaboration with Spark therapeutics investigating SPK-9001. As a snapshot 35 projects are in Phase 1, 34 are being in phase 2, 23 in phase 3, 9 went for registration with a total of 101 (metrics as of July 2019)
Constantly providing medicines in the areas of Hospital (anti infectives), oncology, anti inflammatory, oncology, rare diseases, biosimilars, vaccines and new molecular entities.
Partnering in social responsibility by delivering medicines in remote areas and uplifting the needed areas.
About the Job
Job Location : Chennai
Experience : Candidate need to have experience of 1-3 years with MSc Chemistry
Roles
Interpretation of experiment
Preparation of documents and lab activities
Candidate need to adhere to the trainings and support the MS&T/TT/KGL departments/ Should perform the literature search and develop the robust process and need to resolve the issues during the scaleup, and during the manufacturing process.
Candidate should prepare the reports protocols for the lab activities
For Safety data management specialist
Qualification : B. Pharma only with no more than 2 years
Candidates need to have direct work experience in PV, Individual case safety report (ICSR)
B. Pharma freshers are invited to apply
need to have skills in Pharmacovigilance and analytical skills
Need to have knowledge in E2B case processing and ARGUS safety data base