4,884 Microbiology jobs in India
Microbiology
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Position: Microbiology
Location: Ahmedabad, Gujarat
Shift Timing: Between 7:00 AM to 9:00 PM (9-hour shift)
Experience Level: Fresher or Experienced
Qualification: M.Sc / B.Sc
Key Responsibilities:
- Perform microbiological analysis of raw materials, in-process samples, and finished products.
- Conduct environmental monitoring including air, surface, and water testing.
- Identify and isolate microorganisms using various techniques such as gram staining, culture, and microscopy.
- Maintain and calibrate laboratory equipment and instruments.
- Ensure strict adherence to safety and hygiene protocols.
- Prepare and maintain accurate records, reports, and documentation as per regulatory standards (e.g., GMP, ISO).
- Support product development, validation, and shelf-life studies.
- Assist in investigating non-conformities and implementing corrective actions.
- Collaborate with QA/QC teams and participate in audits when required.
Job Type: Full-time
Work Location: In person
Microbiology
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Microbiologists study microorganisms to solve problems that affect health, the environment, and food and agriculture. They work in a variety of settings, including healthcare, industry, and pharmaceutical development.
Microbiology Analyst
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Job description: Microbiologist - Executive
Company : Sain Medicaments Pvt Ltd – Hyderabad
About the Company:
Sain Medicaments Pvt Ltd is a leading pharmaceutical formulation company, proudly serving Human Healthcare since 1970s, we have come a long way to make a mark in the healthcare, industry which has ISO 22000:2005, WHO GMP, GLP certified manufacturing unit situated at HYDERABAD.
Opening for: Microbiologist
Job Duties:
- Supervise and conduct various microbiological activities on a regular basis.
- Develop and maintain validation in all protocols.
- Perform laboratory analysis on all materials after appropriate sterilization.
- Perform tests on component samples, identify any contamination, conduct an analysis and initiate corrective measures.
- Study various cultures of microorganisms in isolation according to standard inhibition and ensure control over moisture and temperature.
- Monitor all physiological and morphological characteristics and identify microorganisms.
- Perform tests on all incoming ingredients and document all records.
- Perform audits and reviews.
- Develop various testing processes for all raw materials and equipment, and monitor all finished products.
- Investigate all issues and prevent any GMP problems on samples.
- Maintain accurate records and perform tests on all activities conducted in the laboratory.
- Develop and document various microbiology laboratory processes and prepare final reports.
- Maintain purchase orders for all laboratory processes and monitor inventory.
Candidate should have knowledge of the following:
- Serve enthusiastically and represent our laboratory professionally
- Deep knowledge in managing a laboratory project and collaborate with a wide variety of technical colleagues
- Proficiency in numeracy and IT skills
- Strong oral and written communication skills
- Ability to plan and execute experimental protocols.
- Excellent knowledge of electron microscopes, electronic equipment, chemical samples, and stains and weighing equipment.
- Highly skilled in microbiology techniques, methodology, equipment and supplies.
Experience:
- 1-2- years of successful Micro Analytical Laboratory experience ( or Fresher)
Qualification:
- Degree in Microbiology or Biochemistry or related (essential).
- 2 year of experience as a Microbiologist (essential).
Industry
- Pharmaceutical Manufacturing
QC Microbiology
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Department
MORAIYA QC
Job posted on
Aug 29, 2025
Employment type
P-P8-Probationer-HO Executive
Role Name: QC Microbiology (Manager/Senior Manager)
- Division - Moraiya
- Department - QC
- Category - Staff
- Qualification - M.Sc (Microbiology)
- Experience - 15+ Years
- Zydus Experience - Must have completed at least full two PMS cycle with Zydus.
Job Responsibilities:
Lab Compliance:
- Responsible for overall Microbiology functions and 24X7 inspection readiness to laboratory compliance & safety in the laboratory.
- To lead and manage the strategic and operational performance of the quality department, ensuring the successful delivery of business strategy, Key Performance Indicators (KPIs) and objectives, whilst adhering to regulatory compliance and achieving commercial success.
- Responsible for implementing company quality ethics policy for data integrity and inform as per corporate data governance policy.
- To ensure OOS/OOT/OOC/MDD/Deviation/Laboratory incidents are adequately investigated, trended, evaluated and ensure that action items and corrective or preventive actions are identified, addressed, and successfully implemented.
- To ensure the quality systems are maintained in compliance with corporate standards.
- To support CQA for effective implementations of key cGMP initiatives undertaken by various CQA functions.
- To identify system implementation issues and resolves them within and between area management.
- To provide regulatory support on issues to submission/review response related to deficiencies related to analytical testing.
- To ensure all Pharmacopoeias updates for Microbiology general chapter, API, excipients, packing material and drug products
- To ensure adequacy of analytical method validations as per current regulations.
- To ensure stability data generated on submission batches are completed as per the requirements and to ensure compliance of abnormal trends on time.
- To ensure analytical instruments are meeting appropriate regulatory requirements and complying to 21 CFR part 11/EU Annex-11.
- To ensure contract analytical testing facilities are qualified as per regulatory requirement and corporate policies.
- To ensure that section of product testing, non-commercial testing, raw material, packing material, investigation OOS/OOT/MDD/OOC/Incident, lab support and microbiology complies with the regulatory requirement and corporate policies.
- To review quality index/ QUEST index for quality indicating parameters and compliance status of the quality control.
- To review & approve the calibration/stability schedule, working standards & primary standards COA's and release COAs (as applicable).
- To review stability protocols & reports and other qualification protocols & reports.
- To ensure adequate analytical support is provided for any investigation analysis and root cause established for all non-confirmed OOS/ OOT/ OOC (OOS and OOT due to laboratory errors).
- To review OOS/ OOT/ OOC/ Incident for its appropriateness and completeness. To suggest CAPA for laboratory failures as an outcome of OOS/ OOT/ OOC/ Incident investigation.
- To review all trend data (OOS/ OOT/ incidence, microbiological) and initiate appropriate actions wherever necessary in consultation with corporate quality if required.
- To ensure that appropriate measure are taken to prevent recurring of OOS/ OOT.
- To review change control, deviation and associated impact assessment.
- To ensure verification of calibration devices are done at approved, qualified, NABL accredited agency, government laboratory or equivalent laboratory.
- To coordinate with manufacturing/ GDSO/ Regulatory/ Quality Assurance for timely release of raw and packing materials, in-process, semi-finished and finished products.
- To ensure that adequate and appropriate glassware, chemicals, standards, culture media, microbial culture strain & other resources required for analysis are available in the laboratory.
- To ensure appropriate action is taken in case of data integrity issue and perform impact analysis.
- To coordinate with corporate quality for the implementation of applicable regulatory compliance points of other sites to his / her site.
- To ensure annual maintenance contract renewal and calibration of analytical instruments.
- To evaluate the complaint sample & report the result to quality assurance.
- To intimate immediately to Head Quality Control/Quality Assurance about the on-going commercial stability failure.
- To coordinate with external customers for laboratory related issues.
- To provide analytical support in investigations of market complaints and No Standard Quality (NSQ).
- Responsible for review of SOP's in DMS.
- Review/HOD approval in trackwise for QMS and investigation/risk assessment document.
Audit and Compliance:
- To represent Microbiology Department during customer as well as regulatory audits.
- To review compliance reports of regulatory audits.
- To conduct the GEMBA round at site and to prepare the site for external audits.
- To ensure Microbiology labs are compliant to cGMP by assessing the laboratory through periodic audits.
- Responsible to fulfill the compliance to audit commitments completion rate.
- To review the compliance response to the results of product quality system assessments by internal and external auditors and ensure execution as per timelines.
- To ensure implementation of global CAPA's at sites.
Service Level Commitment:
- To ensure all stability samples analysis completed as per schedule and no stability samples are pending beyond timeline.
- To ensure on time analysis and disposition of RM, PM, in-process, finish product and stability samples
- To conduct the vendor audits as and when required.
- To conduct the self-inspection audit of all sites of Zydus.
Resource Management:
- To ensure timely recruitment of resource and to place the right peoples at right place.
- To create KPI for sub-ordinates.
- To mentor and prepare second line as back up.
- To prepare the budget for the Microbiology.
- To ensure system users are qualified by establishing requirements and providing training content.
- To oversight assigned new projects are designed as per the expectations from Quality perspective and implemented as per the plan.
- To ensure adequate resource for training and qualification of analyst.
Working across boundaries:
To interact with R & D and Technology Development for quality development as per QbD guidance and provide necessary support for new products and projects with reference to development and scale up trials.
To effectively implement new technologies, laboratory automation and other initiatives taken by corporate quality.
Assistant - Microbiology
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We are looking for a highly motivated and experienced Assistant in Microbiology to join our team at Vijaya Diagnostic Centre Limited. The ideal candidate will have 1-3 years of experience in the field.
Roles and Responsibility
- Conduct microbial testing and analysis to ensure product quality and safety.
- Develop and implement microbiological protocols and procedures.
- Collaborate with cross-functional teams to achieve project goals.
- Maintain accurate records of test results and inventory management.
- Ensure compliance with regulatory requirements and industry standards.
- Participate in continuous improvement initiatives to enhance laboratory operations.
Job Requirements
- Bachelor's degree in Microbiology or related field.
- Strong knowledge of microbiological techniques and principles.
- Excellent analytical and problem-solving skills.
- Effective communication and teamwork skills.
- Ability to work in a fast-paced environment and meet deadlines.
- Familiarity with laboratory information systems and software.
Technician - Microbiology
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Roles and Responsibility
- Conduct microbial testing and analysis to ensure product quality and safety.
- Develop and implement microbiological protocols and procedures.
- Collaborate with cross-functional teams to achieve project goals.
- Maintain accurate records of test results and inventory management.
- Ensure compliance with regulatory requirements and industry standards.
- Participate in continuous improvement initiatives to enhance laboratory operations.
Job Requirements
- Bachelor's degree in Microbiology or related field.
- Strong knowledge of microbiological techniques and principles.
- Excellent analytical and problem-solving skills.
- Effective communication and teamwork skills.
- Ability to work in a fast-paced environment and meet deadlines.
- Familiarity with laboratory information systems and software.
Microbiology Officer
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Position Microbiology Officer
Ø Location : Boisar
Ø Exp : Min 2 Years (Rel)
Ø Qlf'n : B.Sc (Micro)
Ø Gender : Male
Industry - Pharma Company
Job Role :
· Perform water Analysis, Growth promotion test
· Microbiological Testing: Finish Product
· Environmental Monitoring: Regularly assess cleanroom conditions and ensure sterile environments meet regulatory standards.
· Sample Preparation & Data Analysis: Prepare samples, analyse results, and maintain accurate records
Skills:
· Strong understanding of microbiological techniques and biosafety levels.
· Familiarity with GMP practices and regulatory compliance.
· Proficiency in lab software and reporting tools.
· Good communication and teamwork abilities.
There will be rotational shifts for this postion.
If interested, please share resume on
Job Types: Full-time, Permanent
Pay: ₹15, ₹25,000.00 per month
Benefits:
- Health insurance
- Life insurance
- Paid time off
- Provident Fund
Work Location: In person
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Microbiology Technician
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Walk-in Drive – Microbiology Technician
Venue:
AIG Hospitals, Gachibowli
B2 Block – Admin Department
Dates:
12th September 2025(Friday) to 13th September 2025(Saturday)
Time:
10:00 AM to 1:00 PM
Requirements
- B.Sc. MLT.
- 1–3 years of lab experience preferred.
- Strong knowledge of lab equipment and aseptic techniques.
Important Note:
Registration with a recognized medical laboratory & Paramedical council is mandatory.
Location: Gachibowli, Hyderabad
Department: Microbiology
Type: Full-time
Key Responsibilities
- Conduct microbiological tests (cultures, staining, sensitivity).
- Maintain lab hygiene and sterilization protocols.
- Record and report results accurately.
- Follow NABL and hospital safety standards.
Skills Required
- Proficiency in microbiological techniques and lab equipment.
- Strong documentation and analytical skills.
- Knowledge of cGMP, GLP, and biosafety procedures.
- Ability to work independently and in a team.
- Good communication and problem-solving abilities.
Job Types: Full-time, Permanent
Benefits:
- Health insurance
- Paid sick time
- Paid time off
- Provident Fund
Work Location: In person
Assoc, Microbiology
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This is where your work makes a difference.
At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job—you will find purpose and pride.
- To prepare Standard Operating Procedure (SOP)/documents/Investigation for Microbiology lab and report to Supervisor and Quality Assurance (QA), if the non-conformity is observed.
- To initiate the change in process, equipment or facility as per operational requirement.
- Timely closure of CAPA/NCR/LIR and quality documents related to Microbiology lab.
- To access the impact of functional and cross functional document change control (DCR) or change control management (CCM).
- To perform investigation non-conformity identified.
- To initiate CCM and impact assessment of the cross functions through QMS.
- To prepare error free document as per Corrective and Preventive Action.
- To impart the training to concerned personnel as per requirement.
- To handle QMS documents and relative documentation to its closure in defined timeline.
- To prepare SOP and update according to cGMP requirements or any observation.
- To perform the task, which assigned by the management from time to time.
- To prepare and analyze the non-conformity or Out of Specification line wise.
- To ensure cGMP violation escalation to the Supervisor for their attention and to seek the solution.
- To escalate any non-compliance observed on shop floor to Supervisor.
- To intimate and discuss the non-conformity report and its impact with Supervisor and implement appropriate CAPA.
- Prepare SOP, protocols, standard testing, specification as per the regulatory guidelines
- Coordinate with QA/QC/QMS/Audit & Compliance personnel for implementation of the current / revised standard testing procedures, specifications and method of analysis.
- To handle external & internal audits and ensuring effective implementation of CAPA.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
microbiology tutor
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The Institute of Paramedical Science and Management (IPSM) in Delhi is dedicated to providing quality education in paramedical sciences and hotel management with affordable fees. Managed by The Intellectual Society of India, IPSM is registered under the Registration of Society Act 1860. The institute offers a range of diploma and degree courses aimed at fostering global outlook and expertise among students. IPSM is committed to creating world-class professionals in their respective fields.
Role Description
This is a full-time on-site role located in Dwarka for a Microbiology Tutor. The Microbiology Tutor will be responsible for preparing and delivering lectures, conducting laboratory sessions, assessing student progress, and providing academic support. The tutor will also be required to stay updated with the latest advancements in the field of microbiology and incorporate this knowledge into the curriculum to enhance student learning.
Qualifications
- Strong understanding of microbiology concepts and practical applications
- Experience in teaching or tutoring microbiology at the collegiate level
- Ability to prepare and deliver effective lectures and laboratory sessions
- Excellent written and verbal communication skills
- Ability to assess and evaluate student performance
- Proficiency in using educational technology and resources
- Master's degree in Microbiology or a related field
- Commitment to staying updated with advancements in the field