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
Experience : 4+ years of experience in Microbiology or Biotechnology
Need to have skills in handling the Bacterial endotoxins and micro Assay and sterility testing
Expertise in water monitoring/ testing, and handling of in process, finished and bulk drugs
Need to have quality systems knowledge
Should have broad knowledge in written and verbal kills
Role
Able to Support preparation of media, receipt, storage and handling of Bio ball cultures, and investigations related to microbiology.
Identify the tasks associated with maintaining Current Good Manufacturing Practices {part of GxP} compliant Quality Control and Stability laboratories.
authorize and timely view all laboratory data and have an extensive overall knowledge of all laboratory operations.
Identify the detailing requirements for building, Laboratory Information Management System builds, testing and managing its Master Data changes.
Handling the testing including, but not limited to raw materials, clinical and/or commercial product, stability, validation and Environment Monitoring samples.