Openings in Pfizer for Associate manager in Engineering Investigations

 


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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.


About the Job 

Experience " 5+ years 

Qualification : Bachelors degree 

Able to have experience in solving the investigations from engineering stream and experience in pharma industry

Confortable to work in team and as a individual contributor 

Effective communication skills and presentation skills required 

Experience with writing investigations and using methodology 

Required Method-1 and Human performance investigation training 

Certification of yellow belt is required and handling of quality management tools is required 

Strong understanding of manufacturing and compliance, technical investigations and process systems is required 

Ensure the appropriate compliance with investigations and lead, review the change control of validation and qualifications