Company: Cipla Limited
Position: Junior Team Member – Microbiology
Job Location: Baddi, Himachal Pradesh
Qualification: M.Sc Microbiology
Experience: 1–5 years for Analyst-level responsibilities; 3–7 years for Reviewer-level responsibilities
Job ID: 106534
Posting Date: 31 August 2026
By PharmaBharat Editorial Team | Updated: 31 August 2026
Cipla has announced an opportunity for the position of Junior Team Member – Microbiology at its Baddi facility in Himachal Pradesh. This pharmaceutical microbiology job is suitable for M.Sc Microbiology candidates with relevant experience in microbiological testing, quality control, cGMP documentation, sterility testing, environmental monitoring and laboratory operations.
The Junior Team Member – Microbiology will be responsible for analysing allocated samples, reviewing microbiological results and ensuring that samples comply with predefined microbiological quality specifications and regulatory standards.
Candidates searching for Cipla Microbiology jobs 2026, M.Sc Microbiology jobs in pharma, QC Microbiology jobs in Baddi, pharmaceutical microbiology jobs in Himachal Pradesh, or microbiologist vacancies in the pharmaceutical industry can review the eligibility and responsibilities below.
Job Purpose
The primary purpose of the Junior Team Member – Microbiology position is to perform microbiological analysis of allocated samples and generate reliable, accurate and reproducible results.
The selected candidate will help ensure that samples comply with established microbiological quality parameters, specifications, standard operating procedures and applicable pharmaceutical quality requirements.
Key Responsibilities
Microbiological Sample Analysis
- Analyse microbiological samples according to assigned priorities and work allocation.
- Perform testing according to applicable specifications and approved microbiological methods.
- Review analytical data and microbiological test results.
- Prepare, review and submit reports to the Team Leader within stipulated timelines.
- Support timely sample and batch release while meeting laboratory service-level requirements.
Investigation and CAPA
- Promptly report laboratory errors, abnormal observations and non-compliances.
- Identify issues associated with procedures, instruments and laboratory equipment.
- Initiate investigations wherever required.
- Participate in appropriate corrective and preventive actions (CAPA).
- Investigate laboratory incidents and errors on priority to minimize delays in batch release.
- Help prevent recurrence of microbiological laboratory issues.
cGMP, GDP and GLP Documentation
- Record raw data, observations and findings contemporaneously in relevant test data sheets.
- Maintain complete and accurate microbiology laboratory documentation.
- Review reports according to cGMP and Good Documentation Practices (GDP).
- Ensure laboratory activities comply with applicable GLP requirements.
- Follow approved SOPs and procedures to prevent GMP and regulatory observations.
Laboratory Equipment Management
- Evaluate and document instrument and equipment breakdowns.
- Support investigation of equipment-related issues.
- Recommend measures that may help prevent recurring equipment failures.
- Maintain laboratory equipment and instruments in an optimal condition.
- Help minimize non-compliances arising from instrument or equipment malfunction.
Microbiology Laboratory Operations
The role may involve significant microbiology laboratory activities including:
- Microbial Limit Testing (MLT)
- Sterility testing
- Bioburden testing
- Water sample analysis
- Swab analysis
- Environmental monitoring
- Autoclave operations
- DHS operations
- Media and plate management
- Microbiological documentation and report review
The job description indicates approximately 15 MLT reports daily, 15 sterility batches weekly, 15 bioburden samples, 50 water samples, and environmental monitoring involving approximately 200 locations daily, depending on laboratory requirements and work allocation.
Internal and External Coordination
The Junior Team Member – Microbiology will interact with multiple functions to support efficient laboratory operations.
Internal coordination may include:
- Manufacturing/operational units for specifications, protocols, documents and area availability
- QA and QC teams for product and sample release
- Stores for procurement of required laboratory materials
- Team Leader – Microbiology for daily media and plate requirements
The role may also involve coordination with Corporate Quality Assurance (CQA) for relevant pharmacopoeial guidelines and quality requirements.
Education Qualification
Candidates should possess:
M.Sc in Microbiology
Candidates should ensure that their educational qualification meets the requirements specified in the official job posting before applying.
Experience Required
The job description specifies:
- Analyst: 1–5 years of relevant Microbiology experience
- Reviewer: 3–7 years of relevant Microbiology experience
Candidates with hands-on experience in a pharmaceutical microbiology or Quality Control laboratory environment may be particularly relevant for this opportunity.
Skills Required
Candidates should have:
- Strong knowledge of microbiology
- Pharmaceutical microbiological testing knowledge
- Microbial Limit Testing knowledge
- Sterility testing knowledge
- Bioburden testing
- Water analysis
- Environmental monitoring
- cGMP knowledge
- Good Documentation Practices (GDP)
- Good Laboratory Practices (GLP)
- SOP compliance
- Laboratory investigation skills
- CAPA awareness
- Microbiology laboratory equipment handling
- Accurate documentation skills
- Ability to perform assigned laboratory activities independently
- Good English communication skills
- Ability to work within defined laboratory timelines and SLAs
Why Consider This Microbiology Role?
This opportunity can provide experienced microbiology professionals with exposure to pharmaceutical Quality Control operations involving microbiological testing, environmental monitoring, sterility testing, water analysis and GMP-compliant documentation.
The role also provides practical exposure to laboratory investigations, CAPA activities, sample release processes, equipment management and coordination with QA/QC and manufacturing functions.
For candidates building a long-term career in pharmaceutical microbiology, Quality Control Microbiology, sterility assurance or pharmaceutical quality, the responsibilities are directly aligned with core microbiology laboratory functions.
Who Can Apply?
This opportunity is primarily suitable for candidates who:
- Hold an M.Sc in Microbiology
- Have relevant pharmaceutical microbiology experience
- Have approximately 1–5 years of experience for analyst responsibilities
- Have approximately 3–7 years of experience for reviewer responsibilities
- Understand microbiological testing procedures
- Are familiar with GMP-regulated laboratory environments
- Can maintain accurate and contemporaneous laboratory documentation
- Have good written and verbal English communication skills
Job Location
Baddi, Himachal Pradesh, India
Baddi is one of India’s major pharmaceutical manufacturing hubs and hosts manufacturing facilities of numerous domestic and multinational pharmaceutical organizations.