Testimonials

  • Pinned
    Vijaykumar was very energetic and active person he thinks always out of the Box He is Good influencer he is very diligent, pro-active and focused hard worker.
    Ramesh RK
  • This pdf is very helpful and highly recommended for knowledge related to pharmaceutical microbiology.
    Dhwani Rathod
  • The contents were exttemely useful
    ANAND M P
  • According to my knowledge, Better to keep key points in every parameter of microbiology topic individually,then it would be appreciated and expecting more and more Insightful topics related to micro especially method validations.thank you Vijay ji.
    Nalla Sanjeev
  • Helpful
    Anonymous

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Video meeting . 30 mins
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7+years of experience in microbiology QC
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4.5/5
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Testimonials

About me

6 years of experience in quality control microbiologist reputed pharmaceutical industry . Perform the routine/ non-routine environmental monitoring. handling of TOC instrument and calibration. calibration of micropipette and internal instruments calibration all equipments. incubator PLC reports verification. Documents Review. Sampling and testing of water, pure steam, Drain, Rinse, Equipments swabs. Compressed air and nitrogen gas monitoring. Good documentation and data entry of all test results. Preparation of purified water, treated water and environmental monitoring monthly and yearly trends. preparation of microbial media, sterilization and growth promotions. Used media disposition after decontamination. Isolation and identification of in house isolates. perform data entry into the laboratory information management system (LIMS) instruments handling like TOC, Air sampler,Balance, pH meter, Incubators, vertical autoclave, HPHV, colony counter, water batch, water activity analyser,LAF, Biosafety cabinet. Support investigations for Excursion, Deviations. Coordinate with suppliers of microbiological media and other equipments. Department for training needs and technical support. Perform duties as assigned by QC manager or designee. Compliance to GMP, GDP, GLP. Reporting of Deviations,out of action/ Alert limites and LIR in the laboratory. Experience in complying and implementing standard operating procedures. Successfully faced the audit by USFDA. A detail oriented hard working, well organized, self starter and committed to top quality work. My skills and experience can effectively utilised for my personal and organisations growth. computer skills: Microsoft office LIMS