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Microbiology Job Opening at Cipla

Are you looking for a rewarding Microbiology Job in the pharmaceutical industry? Here’s an exciting opportunity through Cipla Careers for talented microbiology professionals seeking growth in quality control and laboratory operations. This Life Science Careers opportunity offers hands-on exposure to microbiological testing, environmental monitoring, sterility analysis, and GMP-regulated pharmaceutical processes. If you hold an M.Sc. in Microbiology and want to build a successful career in pharma quality testing, this role could be your perfect next step.

About Cipla

Cipla is one of India’s leading pharmaceutical companies with a strong global presence across multiple therapeutic areas. The company is known for its commitment to quality, innovation, and affordable healthcare solutions. Through Cipla Careers, professionals gain opportunities to work in world-class manufacturing, research, quality control, and regulatory environments while building successful Life Science Careers.

Position Details

Particulars Details
Job Title Junior Team Member – Microbiology
Country India
State Sikkim
Location Rangpo
Requisition ID 104420
Department Microbiology
Industry Pharmaceutical / Life Sciences
Experience Required 1–5 years (Analyst) and 3–7 years (Reviewer)
Educational Qualification M.Sc. Microbiology
Job Type Full-Time

 

Job Overview

A vacancy is available for the position of Junior Team Member – Microbiology at Rangpo, Sikkim, India. The role is responsible for executing microbiological analysis of allocated samples and producing reliable and reproducible results to ensure compliance with microbiological quality parameters, predefined specifications, and applicable standards.

The incumbent will support timely sample analysis, report generation, laboratory compliance, equipment maintenance, and batch release activities while adhering to cGMP, GDP, and GLP requirements.

Microbiology Job Purpose

The Junior Team Member – Microbiology is responsible for:

  • Executing microbiological analysis of allocated samples.
  • Producing reliable and reproducible test results.
  • Ensuring compliance with microbiological quality requirements.
  • Supporting timely sample release as per defined service level agreements (SLAs).
  • Maintaining laboratory compliance with applicable quality and regulatory standards.

Key Accountabilities

Key Accountability 1: Sample Analysis and Review

Objective

Analyze and review allocated samples to meet service level agreements and support timely sample release.

Responsibilities

  • Analyze samples according to assigned priorities and work allocation.
  • Review generated data against:
    • Approved specifications
    • Microbiological methods
    • Obtained analytical results
  • Prepare, review, and submit reports to the Team Leader within stipulated timelines.
  • Support individual sample release within agreed timelines to achieve SLA requirements.

Key Accountability 2: Error Reporting and Investigation

Objective

Report errors, abnormal observations, and non-compliances promptly to facilitate timely corrective actions and avoid delays in product release.

Responsibilities

  • Report abnormalities related to:
    • Procedures
    • Equipment
    • Instruments
    • Laboratory operations
  • Initiate investigations when deviations occur.
  • Implement corrective and preventive actions (CAPA).
  • Investigate laboratory errors and incidents on a priority basis.
  • Ensure timely batch release and prevent recurrence of issues.

Key Accountability 3: Documentation and Compliance

Objective

Maintain accurate documentation and ensure compliance with laboratory quality standards.

Responsibilities

  • Record entries, raw data, and findings contemporaneously in relevant test data sheets.
  • Facilitate laboratory QA review through complete and accurate documentation.
  • Avoid missed entries and documentation errors.
  • Review reports for compliance with:
    • cGMP (Current Good Manufacturing Practices)
    • GDP (Good Documentation Practices)
    • GLP (Good Laboratory Practices)
  • Follow approved SOPs and procedures.
  • Ensure no GMP or regulatory observations arise due to non-compliance.

Key Accountability 4: Equipment and Instrument Maintenance

Objective

Ensure optimal functioning of laboratory equipment and instruments.

Microbiology Job Responsibilities 

  • Evaluate and document equipment and instrument breakdowns.
  • Recommend preventive mechanisms to minimize equipment failures.
  • Maintain equipment and instruments effectively.
  • Prevent incidents or non-compliances resulting from equipment malfunction.

Key Accountability 5

Details not specified in the provided job description.

Key Accountability 6

Details not specified in the provided job description.

Major Challenges

The role may encounter the following challenges:

  • Validation Record Availability: Availability of validation records for analysis samples may be challenging when validations are conducted at other sites.
  • Resource and Material Constraints: Material and resource availability may be affected by conflicting priorities between laboratories.
  • Coordination among analysts may become challenging while maintaining service level agreements.

Key Interactions

Internal Interactions

The incumbent will interact regularly with:

  • Manufacturing and Operational Units
    • For:
      • Receiving specifications
      • Documentation
      • Protocols
      • Area availability
      • Daily operational support
  • Quality Assurance (QA) and Quality Control (QC)
    • For:
      • Product sample release
      • Daily coordination
  • Stores Department
    • For:
      • Procurement of laboratory materials
      • Need-based requirements

Additional Communication

Communicate observations identified in specifications or testing processes.

External Interactions

  • Central Quality Assurance (CQA)
    • For:
      • Procuring pharmacopoeial guidelines
      • Need-based technical support

Performance Dimensions

The role is expected to manage and support the following activities:

  • Daily Activities
    • Review and release approximately 15 MLT reports per day to achieve SLA requirements.
    • Release approximately 200 environmental monitoring locations daily.
  • Weekly Activities
    • Review and release approximately 15 sterility batches per week.
    • Review and release approximately 15 bioload samples per week.
  • Additional Laboratory Activities
    • Analyze and release approximately 50 water samples.
    • Prepare approximately 10 Technical Information Sheets for swap analysis.
    • Perform 6 Autoclave and DHS operations.

Key Decisions

Recommendations

The incumbent will provide recommendations regarding:

  • Daily media requirements.
  • Daily plate requirements.

Recommendations will be communicated to the Team Leader – Microbiology.

Educational Qualification

Required Qualification

Candidates must possess:

  • M.Sc. in Microbiology

Relevant Work Experience

Analyst Level

  • 1 to 5 years of experience in Microbiology.

Reviewer Level

  • 3 to 7 years of experience in Microbiology

APPLY ONLINE HERE

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