Microbiology Technician

Sterling Accuris Wellness

Ahmedabad District

On-site

INR 240,000 - 300,000

Full time

14 days+
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Job summary

Sterling Accuris Wellness seeks a skilled laboratory technician to ensure quality and integrity of specimens, process cultures, and perform microbial identifications. You will work with LIMS, maintain records, and follow SOPs in a NABL/ISO/CAP compliant environment.

The role requires aseptic technique, routine instrument maintenance, and timely reporting of results, with strict adherence to QC/EQAP protocols and documentation throughout the workflow.

Qualifications

  • Experience with NABL/ISO/CAP quality requirements and documentation.
  • Proficiency in maintaining accurate records and logs across all steps.
  • Familiarity with quality control processes (IQC/EQAP) and corrective actions.
  • Ability to operate and validate equipment and instruments per SOPs.
  • Knowledge of LIMS usage, data entry, validation and report generation.

Responsibilities

  • Check specimen quality and integrity before processing and notify concerns.
  • Process bacterial, TB, fungal cultures and sensitivity per procedures.
  • Identify microbes using biochemical tests, microscopy, staining, and automated systems.
  • Conduct antimicrobial susceptibility testing.
  • Perform aseptic techniques in laminar flow hoods or biosafety cabinets.
  • Maintain equipment and fill maintenance logs daily.
  • Prepare media, reagents and buffers; maintain records.
  • Follow instrument and reagent manufacturer instructions.
  • Ensure timely QC, EQAP and documentation.
  • Document corrective actions for QC/EQAP failures.
  • Manage time to ensure timely report release.
  • Record results in log books/registers and verify in LIMS.
  • Fill lab records for easy retrieval and NABL/ISO/CAP compliance.
  • Monitor instruments for breakdowns and environmental conditions.
  • Report breakdowns to Biomedical engineer/ Admin.
  • Ensure prompt processing and reporting of STAT samples.
  • Maintain departmental stock through coordination with supply chain.
  • Submit quality indicator data to QA as requested.
  • Handle receipt, consumption and disposal of reagents per processes.
  • Draft and review SOPs; keep them updated for accuracy.
  • Understand clinical aspects of tests performed in the section.
  • Follow BMW management procedures for reagents.
  • Ensure accuracy of results via SOPs, calibration, QC, and training.

Skills

Quality control
Documentation
Instrument maintenance
LIMS knowledge

Tools

LIMS software
Laminar flow hood
Biosafety cabinet
Automated systems

Job description

  • 1. Checking the specimens quality and integrity before processing and notify concerned person about any issues identified. Ensuring adequate clinical information in the accompanying requisition form.
  • 2. Processing of bacterial, TB, fungal culture, and sensitivity as per laboratory defined procedure or reagent package inserts.
  • 3. Perform microbial identification using biochemical tests, microscopy, staining techniques, and automated systems.
  • 4. Conduct antimicrobial susceptibility testing.
  • 5. Perform aseptic techniques and work in laminar flow hoods or biosafety cabinets when required.
  • 6. Perform routine maintenance of equipment's and fill-up the maintenance logs on daily basis.
  • 7. Preparing media, reagents and buffers and maintain records of the same.
  • 8. Review & follow instrument & reagent manufacturer's instructions.
  • 9. Ensuring timely and regular performance of Quality control & EQAP and documentation.
  • 10. Corrective action documentation in case of failure in IQC or EQAP.
  • 11. Time management to ensure accurate and timely report release.
  • 12. Recording the results, in respective log books/registers counterchecking and ensuring timely correct typing & Validation in LIMS.
  • 13. Systematic filling of lab records for easy retrieval and maintaining records as per NABL/ISO/CAP requirements.
  • 14. Constant monitoring of instruments for any breakdowns error flags and temperature & environment condition monitoring logs.
  • 15. Reporting the breakdowns to Biomedical engineer / Administrative department.
  • 16. Ensuring prompt processing and reporting of TAT & STAT samples.
  • 17. Maintain departmental stock as per requirement by coordinating with Supply chain & store team.
  • 18. Submit quality indicator data form to quality assurance as and when requested.
  • 19. Follow the system of receiving, consumption & discard of reagents as established by supply chain & top management.
  • 20. Responsible for drafting new Standard Operating Procedures (SOPs), updating existing ones as needed, and conducting regular reviews to ensure accuracy and compliance.
  • 21. Understanding clinical aspects of tests conducted in the section.
  • 22. Follow laboratory procedure for BMW management.
  • 23. Ensuring accuracy and correctness of results by strict compliance to the defined standard Operating procedure, calibration, quality control, procedure and training of the personnel.
  • 24. Reagent Calibration for each new LOT & reagent LOT Verification for each new LOT / Shipment.
  • 25. Participate in training & continual education programs conducted by organization and quality assurance team.
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