Gland Pharma Urgent Requirement For API QC Microbiology Department Date Posted 10th June 2021


Gland Pharma Urgent Requirement For API QC Microbiology Department. If you find this requirement suitable, Apply online from given below link. Keep visiting our website for latest Pharma Jobs.

Job Category: Pharma/Bio tech

Company Name: Gland Pharma

Experience: 2-5 Years

Job Location: Visakhapatnam

Date of Joining: Immediate Joiners

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Job Description:

  • Responsible for sampling, testing and documentation of MLT samples of finished and stability samples.
  • Responsible for Handling of Instruments like LAF/BOD incubators/BET Incubators/Autoclave/colony counter /Microscope/pH meter /Air sampler and Vitek etc.
  • Responsible for monitoring and review of daily printouts of instruments like incubators, Autoclaves, refrigerators, hot air ovens and deep freezers.
  • Responsible for ensuring the destruction of used media plates/tubes, product plates/tubes, monitoring plates, GPT plates/tubes and IND plates/tubes.
  • Responsible for ensuring the handling, calibration of Instruments like pH meter and top pan balance.
  • Responsible for ensuring external calibration review of standard weights used in Microbiology laboratory.
  • Responsible for ensuring the receipt, storage and handling of ATCC cultures/cryovials/bio balls.
  • Responsible for Preparation of Reagents and standard solutions.
  • Responsible for Preparation of SOPs and ensure that complies in microbiology laboratory.
  • Responsible for water analysis and trends for microbiology samples as per schedule.
  • Responsible for procurement of media, microbiology laboratory materials etc.
  • Responsible for ensuring verification of instrument preventive maintenance schedules for incubators, autoclaves, LAFs, air samplers, hot air oven, refrigerator and deep freezer, Colony counter and Vitek.
  • Responsible for, Storage and Retrieval of all microbiology records.
  • Responsible for MLT method validations, and other validation studies.
  • Responsible for Perform and verify Environmental monitoring at sterile and non-sterile production blocks.
  • Responsible for sampling of sterile finished products.
  • Responsible for planning shifts and work allocation for microbiology personnel.
  • Responsible for QMS activities OOS, OOL, Deviations and incidents.
  • Responsible for ensuring training to juniors and Designees.
  • Responsible for ensuring all documents Review in Microbiology laboratory.
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Eligibility Criteria:

  • Note: Only male candidates required for Shifts
  • Required Candidate profile: API QC Microbiology Experience is mandatory
  • 2.0 to 4.50 LPA

Apply Here: Click Here

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