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 and 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
Associate - Microbiology
Experience : 0-4 years experience with masters Degree in microbiology
Location : Vizag
required to have experience in media preparation testing of microbial count
ability to read and understand the compendial methods and handling of standard operating procedures Governmental regulations and technical procedures
require to review and standardize the operating procedures as well as micro biological related procedures keep them in a current version
able to conduct and handle the preparation of microbiological protocols and handling of complex projects to meet aggregate targets and timelines for work activities within a team
need to have strong knowledge on microbiological techniques lean manufacturing 6 Sigma Methodologies and statistics
Able to perform analysis of raw materials related components and finished products required to review and improve the data in computerized systems and generate the reports
Required to have expertise in good manufacturing practice's and its application standards process and policies able to do multitasking and need to have excellent organizational skills
required to manage receipt and store bio ball cultures and able to ensure the records are updated and correctly filled as per the requirement of good documentation practice's
Able to evaluate and interpret the data in terms of accuracy and review the trends against good manufacturing practice's and their impact able to perform and recommend the appropriate corrective actions.
handling and maintenance of master culture associated with isolates and Cryo vials
performance analysis analysis and able to review the complex projects and manage to and record the results the results to reflect the current testing capabilities.
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Apprentice in Validation
Qualification : Masters in Pharma
required to update the platform for healthcare professionals according to the internal regulatory requirements and policies
need to ensure and manage the professional development and accountable and priorities the workflow
required to maintain local documentation as per the regulations and and collaborate with the area manager to develop the digital calendars and approval in different channels
able to ensure the accountability for the higher level of compliances to norms procedures and policies
able to support for marketing teams in the execution of campaigns optimization of digital campaigns and management of reports.
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Quality assurance associate
Location of the Job : Vizag
candidate required to have experience at a manufacturing site and writing and handling deviations experience in production batch manufacturing review investigation of nonconformance handling of root cause analysis and change control management
required to have experience in quality administrative systems and current good manufacturing practises ability to work in team as well as on own
required to handle patch startup and end activities like censor challenges recipe review and perform quality level sampling recording and inspection of results in batch records for all the products
able to identify the gaps involved in the process and procedures update the simplification process thereby reducing the down time and increasing the efficiency
need to perform daily work through and handle the observations and report it to the supervisor
assess and review the recruitment alarms daily as well as quarterly trends
review the SOP and reports as per regulatory requirements and CGMP practises, perform the equipment audit trials and review the batch reports.
perform acceptable quality sampling and record the results in batch records for all the products as well as inspect the lines and perform random cheques for terminal sterilization packing and visual inspection
required to review the equipment breakdown with respect to product quality and patient safety with technical support and inputs from senior specialist or supervisor
able to troubleshoot the abilities in the manufacturing areas and help and help the organization to develop implement and achieve the goals mission and their values
required to have experience and hands on the exhibit batch records and SS the impact of exceptions with technical support and input from supervisor or senior specialist
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