Job Description

• Candidate should have good knowledge about all microbiological related activity, Environmental monitoring of classified areas, Water testing Bioburden BET and Sterility.
• Environmental monitoring of all classified areas of Drug product manufacturing.
• Media Preparation required for Utility and area monitoring.
• To execute Validation/Qualification/Re-qualification as per protocol.
• Sub culturing, serial dilution of standard cultures and GPT and Identification of isolate.
• To execute IQ/OQ/PQ of the new equipment installed in the Microbiology Section.
• Sampling, Testing of Water samples
• To perform Population Determination of Biological Indicators.
• Operation of Daily pH, Balance Calibration, Autoclave, DHS, Incubators, Air Samplers and particle counter.
• To report any Deviations/ Out of Specifications results and Safety risks to the supervisor as and when observed.
• Candidate should have good experience in the BET testing by using Gel clot and KTA method
• To perform Qualification of Equipment, Autoclave, DHS, Incubator, KTA, etc.
• The candidate should be familiar with cGMP requirements, Change Control, Deviations, Out of Specifications, Sample management, Stability Management and investigation tools.
• To perform Compressed air sampling and analysis
• To ensure cGMP compliance and maintain the laboratory in audit ready condition.
• The candidate should be familiar with SAP system.

Work Experience
0 to 2 years
Education
Post Graduation in Microbiology or Biotechnology
Competencies