microbiological analyst

Hcm International

Job Summary:Responsible for ensuring product safety and quality through microbiological testing, system compliance, and adherence to food safety standards. The role involves conducting microbiological analyses, maintaining lab operations, and supporting continuous improvement initiatives within QA systems.Key Responsibilities:Perform microbiological testing of raw materials, in-process, and finished products (TVC, E. coli, Salmonella, Yeast &amp; Mold, etc.).Prepare and maintain microbiological media, chemicals, and testing equipment.Conduct GMP and line clearance audits and verify OPRP/CCP records.Maintain documentation and traceability as per ISO/FDA and food safety standards.Conduct hygiene, housekeeping, and food safety trainings for production staff.Support internal audits, environment monitoring, and continuous improvement activities.Qualifications &amp; Skills:M.Sc. Microbiology / Biotechnology or B.Sc.Strong knowledge of microbiological methods, GMP, and food safety systems.Skilled in data analysis and laboratory practices.Good communication and problem-solving skills.Job Type: Full-timePay: Rs70,000.00 - Rs80,000.00 per monthWork Location: In person

Microbiologist

Glenmark Pharmaceuticals

<div>No Visa Sponsorship: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Glenmark is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity) with eight molecules in various stages of clinical development. The company has a significant presence in branded generics markets across emerging economies including India. Its subsidiary, Glenmark Generics Limited has a fast growing and robust US generics business. The subsidiary also markets APIs to regulated and semi-regulated countries.
POSITION SUMMARY :
The Microbiology Analyst is responsible for performing microbiological tests that support the release of intermediates and finished products. These include routine and non-routine microbiological tests on in-process and final container products, as well as environmental monitoring samples. This position also contributes to the completion of regular routine technical tasks.
JOB RESPONSIBILITIES :
Help maintain inventory by reporting needed supplies. Take appropriate steps to reduce wastages and losses in the Microbiology department.
<ul><li>Monitoring samples, in-process product samples, raw materials, and environmental monitoring (EM) samples.</li>
<li>Successfully complete a gown qualification program to enter and work inside the aseptic manufacturing area.</li>
<li>Perform critical manufacturing process interventions for viable and non-viable EM.</li>
<li>Maintain sample logs on a daily basis to ensure timely testing and tracking of all samples.</li>
<li>Perform routine sampling of critical process utilities (e.g., Water-for-Injection, Purified Water, Clean Compressed Air, Nitrogen Distribution System, etc.)</li>
<li>Count colony forming units (CFU) on Petri plates.</li>
<li>Perform sterility testing on final products and raw materials.</li>
<li>Perform Growth Promotion and Biological Indicator testing.</li>
<li>Perform preparation of reagents, materials, and equipment used in microbiological testing in sterile environments, such as HEPA hoods.</li>
<li>Maintain accurate and complete test records.</li>
<li>Enter test results in the Laboratory Information Management Systems (LIMS).</li>
<li>Maintain Instrument Usage and Calibration Logs based on instrument usage during the preparation and testing of samples.</li>
<li>Maintain current knowledge of regulatory and industry standards, trends and advancements.</li>
<li>Other duties as identified by direct supervisor</li>
<li>Preparation, review and approval of sampling matrix and hold time schedule Conducts and communicates results of lab investigations when test results fall outside pre-established specifications and/or limits (OOS/OOL).</li>
<li>Performs routine equipment maintenance.</li>
<li>Performs maintenance of spare parts inventory, calibrations and supervises third party maintenance and repair when necessary.</li>
<li>Establishes good working relation with contract laboratories.</li>
<li>Supports in the development of methods transfer and validation, troubleshooting, cross validation, IQ/OQ protocols.</li>
<li>Supports activities regarding audits of suppliers and contract labs in support of vendor certification program.</li>
<li>Conducts statistical evaluation of the manufacturing and inspection process and training QC staff.</li>
<li>Assures laboratory databases are maintained and accurate.</li>
<li>Ensures control of laboratory documentation (Raw Material COA, testing instructions, testing.</li>
<li>Ensure that all equipment is calibrated.</li>
</ul>
Education :
<ul><li>Minimum BS/BA in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or equivalent.</li>
<li>Microbiology degree preferred</li>
</ul>
Experience :
<ul><li>1-3 years of experience in a cGMP/GLP laboratory.</li>
<li>Pharmaceutical &amp; FDA/GMP industry experience is preferred.</li>
<li>Microbiology laboratory experience, such as aseptic techniques required</li>
</ul>
Knowledge and Skills :
<ul><li>Knowledge of current cGMP regulations for laboratory setting</li>
<li>Proficient in Windows, Microsoft Word, Excel.</li>
<li>Good written, verbal, and communication skills.</li>
<li>Good documentation skills.</li>
<li>Strong organizational skills.</li></ul></div>

Microbiology Analyst

Refined Reports Data

Key Responsibilities:<ul><li>Research and Analysis:</li><li>Conduct experiments to study microorganisms (bacteria, viruses, fungi, etc.) in controlled laboratory settings.</li><li>Investigate the interactions between microorganisms and human/animal/plant systems.</li><li>Perform genetic, biochemical, and microbiological analyses of samples.</li><li>Develop methods for isolating, identifying, and cultivating microorganisms.</li><li>Data Collection and Interpretation:</li><li>Analyze results from microbiological tests and research to identify patterns and implications.</li><li>Maintain accurate records of research findings, including laboratory notes, test results, and statistical data.</li><li>Utilize advanced software and technologies for data analysis and interpretation.</li><li>Microbial Culture and Identification:</li><li>Grow and maintain microbial cultures under various conditions (e.g., temperature, pH, salinity) to identify new strains or pathogens.</li><li>Prepare culture media and reagents for microbiological experiments.</li><li>Use microscopes, petri dishes, and other lab equipment to study microorganisms.</li><li>Quality Control and Safety Compliance:</li><li>Ensure compliance with safety standards and laboratory protocols, particularly in handling pathogenic microorganisms.</li><li>Develop and implement quality control measures to ensure the accuracy and reliability of test results.</li><li>Supervise laboratory technicians and assistants.</li><li>Reporting and Documentation:</li><li>Prepare detailed reports and research papers for publication in scientific journals or internal use.</li><li>Communicate findings to colleagues, clients, or stakeholders through presentations and meetings.</li><li>Assist in the preparation of grants and funding proposals for future research projects.</li><li>Collaboration:</li><li>Work with other scientists, clinicians, or regulatory bodies to contribute to broader scientific initiatives or public health goals.</li><li>Provide technical advice on microbiological issues to other departments, organizations, or public health agencies.</li><li>Skills and Qualifications:</li><li>Education:</li><li>Bachelor's degree in Microbiology, Biology, or a related field (entry-level).</li><li>Master's or Ph.D. in Microbiology or a specialized field may be required for advanced positions.</li><li>Technical Skills:</li><li>Strong understanding of microbiological laboratory techniques, including culturing, staining, and microscopy.</li><li>Proficiency in using laboratory equipment (e.g., autoclaves, PCR machines, spectrophotometers).</li><li>Familiarity with data analysis software (e.g., SPSS, R, Microsoft Excel).</li></ul>Job Types: Full-time, Permanent, FresherPay: ₹25,465.78 - ₹40,040.66 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Provident Fund</li></ul>Work Location: On the road

Nestlé

<div>Main Purpose of Job
You will be responsible for quality control microbiology testing of product materials and purified water as well as performing environmental monitoring. 
Responsibilities:<ul><li>
Perform and document in-house microbiological testing on raw materials, semi-finish, and finish product according to the established standard operating procedures and approved protocols.</li><li>
Prepare necessary standards, solutions, reagents, media, and samples for sample analysis.</li><li>
Accurately record observations and perform data reviews and release inspection lot in the material management system.</li><li>
Operates and maintains laboratory instruments, while ensuring the reliability of instrumentation through proper maintenance, with ability to troubleshoot minor issues.</li><li>
Must participate and lead continuous improvement using lean principles to assist with streamlining and making the laboratory efficient.</li><li>
Handling all paper works such as Reports.</li><li>
Prepare check receiving reports according to the accurate specs.</li><li>
Reporting of abnormalities via notification of quality deviations and take immediate corrections.</li><li>
Adhere to the Nestle SHE rules and procedures at all times during the working hours to ensure own and others safety.</li></ul>
Requirements:<ul><li>
Bachelor&rsquo;s degree on Microbiology or related major.</li><li>
 More than 1 year of experience in the same position.</li></ul> 
Skills:<ul><li>
Good math's and English skills.</li><li>
proficient in relevant computer applications such as MS Office.</li><li>
Accurate and organize.</li><li>
Ability to work under pressure.</li></ul></div>

Horizon Biolabs Pvt Ltd

Job DescriptionHorizon Biolabs Pvt Ltd. is a GLP compliant Pharmaceutical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices and packaging Industries .We are looking for :Candidate with Msc/Bsc/Bpharm/Mpharm having minimum 03-05 years of experience in any reputed Pharma Testing Lab/ CRO /Pharmaceutical Industry as a Sr.QC Analyst.About the jobThe Quality Control Analyst will report to the Manager of Quality.Experience<ul><li>3+ years of QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.</li><li>Must have hands on experience on HPLC/GC (Gas Chromatography)</li><li>Method Development/validation experience desirable.</li></ul>Education<ul><li>Bachelor&rsquo;s /Masters degree in Science related field required.</li></ul>Job Type: Full-timeSchedule:<ul><li>Day shift</li></ul>Education:<ul><li>Msc/M Phrama/B Pharma/Bsc(Chemistry)</li></ul>Experience:<ul><li>total work: 03-05 years (Required)</li><li>Candidates from QC lab experience in CRO/pharmaceutical industry in a cGMP environment is required.</li></ul>Job Type: Full-timeBenefits:<ul><li>Provident Fund</li></ul>Location:<ul><li>Hyderabad, Telangana (Preferred)</li></ul>Work Location: In personJob Type: Full-timeBenefits:<ul><li>Provident Fund</li></ul>Application Question(s):<ul><li>Are you currently staying in Hyderabad?</li><li>Are you having QC lab experience in CRO/pharmaceutical industry in a cGMP environment?</li><li>are you ready to join immediately?(within 7 days)</li></ul>Work Location: In personJob Type: Full-timeBenefits:<ul><li>Provident Fund</li></ul>Work Location: In person

QC Analyst-HPLC,GC

Sandoz

<div>
 
 
 Job Description
 
 
 
 
 
 Major accountabilities:
 
 
 
 <ul>
 <li>
 OOx/Deviation handling.
 </li>
 <li>
 CAPA definition -KPI trending -Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) Stability -Stability testing (Projects) &ndash; protocol preparation, evaluation, report preparation.
 </li>
 <li>
 Reporting (Stability plan preparation, trend analysis, evaluation)
 </li>
 <li>
 Performance of Stability studies, protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release)
 </li>
 <li>
 Microbiological QC -Perform Microbiological testing of materials and utilities, environmental and personnel monitoring -Provide expert Support for site qualification and validation activities -Maintain and calibrate equipment incl. plan preparation -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)
 
 
 </li>
 </ul>
 
 
 Job Description:
 
 
 
 
 <ul>
 <li>
 To prepare, update, and track revisions of laboratory procedures in accordance with current and legal regulatory guidelines.
 </li>
 <li>
 To work in compliance with current GMP rules and company procedures.
 </li>
 <li>
 To conduct and report necessary activities within the quality management system (OOS/OOT, Deviation Investigation, Change Control, and Corrective and Preventive Actions).
 </li>
 <li>
 To perform and report microbiological analyses of raw materials, semi-finished products, finished products, and packaging materials.
 </li>
 <li>
 To carry out and report the microbiological method validation and verification studies.
 </li>
 <li>
 To implement the environmental monitoring program, evaluate results, and report findings.
 </li>
 <li>
 To perform and evaluate the microbiological controls of compressed air systems.
 </li>
 <li>
 To perform and evaluate microbiological analyses of the water system.
 </li>
 <li>
 To perform microbiological analyses of detergents and disinfectants used.
 </li>
 <li>
 To perform, evaluate, and report disinfectant efficacy studies in accordance with pharmacopeia and related standards.
 </li>
 <li>
 To prepare all culture media and solutions used in the laboratory according to instructions and to perform growth promotion studies.
 </li>
 <li>
 To prepare for and participate in customer and regulatory audits.
 </li>
 <li>
 To conduct and report Microbiological Risk Assessments and OPEX studies.
 </li>
 <li>
 To perform bulk holding time (BHT) studies, evaluate results, and report findings.
 </li>
 <li>
 To ensure the calibration and verification of used equipment are carried out and tracked.
 </li>
 <li>
 To support the qualification and calibration processes of laboratory equipment.
 </li>
 <li>
 To ensure the regular and effective operation of the microbiology laboratory.
 </li>
 <li>
 To ensure the preparation of periodic trend reports and their timely implementation.
 </li>
 <li>
 To ensure that laboratory records are accurate and complete.
 </li>
 <li>
 To track, prepare, and report reference cultures of microorganisms.
 </li>
 <li>
 To perform and report microorganism identifications.
 
 
 </li>
 </ul>
 
 
 Key Performance Indicators:
 
 
 
 
 <ul>
 <li>
 The relevant KPIs that are defined in the Quality Control areas apply: e.g. analytical lead times -Timely and GMP-compliant analysis &amp; documentation of the results.
 </li>
 <li>
 Error rate: Number of OOS (analysis errors) related to the number of analyzes -No complaints about official inspections.
 </li>
 <li>
 Individual performance is assessed using the PMP performance dialog together with the manager
 
 
 </li>
 </ul>
 
 Minimum Requirements:
 
 
 Work Experience:
 
 
 
 <ul>
 <li>
 Functional Breadth.
 </li>
 <li>
 Preferably at least 4 years of experience in a microbiology laboratory, particularly in the pharmaceutical industry (especially in non-sterile manufacturing).
 </li>
 <li>
 Collaborating across boundaries.
 </li>
 <li>
 A GMP environment/equivalent.
 </li>
 <li>
 Bachelor&rsquo;s degree in Microbiology, Biology, Molecular Biology &amp; Genetics, or Bioengineering from the university.
 </li>
 <li>
 Good command of English (reading, writing, speaking).
 </li>
 <li>
 Knowledge and experience in microbiological analysis techniques (e.g., disinfectant efficacy studies, non-sterile product analysis tests, etc.).
 </li>
 <li>
 Proficiency in MS Office programs.
 
 
 </li>
 </ul>
 
 
 Skills:
 
 
 
 
 <ul>
 <li>
 Continuous Learning.
 </li>
 <li>
 Dealing With Ambiguity.
 </li>
 <li>
 Decision Making Skills.
 </li>
 <li>
 Gxp.
 </li>
 <li>
 Industry Standards.
 </li>
 <li>
 Laboratory Equipment.
 </li>
 <li>
 Laboratory Excellence.
 </li>
 <li>
 Quality Control (QC) Testing.
 </li>
 <li>
 Quality Control Sampling.
 </li>
 <li>
 Self-Awareness.
 </li>
 <li>
 Technological Expertise.
 </li>
 <li>
 Total Quality Management.
 </li>
 <li>
 Team-oriented, with strong communication skills, responsible, and detail-oriented.
 </li>
 <li>
 Possesses problem-solving and analytical thinking skills.
 </li>
 <li>
 Able to keep up with the busy work tempo
 
 
 </li>
 </ul>
 
 
 Languages:
 
 
 
 
 <ul>
 <li>
 English.
 </li>
 </ul>
</div>

Sr. Microbiogy Specialist

Voyage Freight.co

The Quality Analyst responsible for ensuring that all grain products meet company and regulatory quality standards. This role involves inspecting, testing, and monitoring grain quality from procurement to storage and distribution. The Quality Officer will work closely with suppliers, production teams, and regulatory agencies to maintain high-quality standards.Note: Candidates must be from Mailsi, Sahiwal, Kamalia, or Pakpattan locations.&middot; Ensure all grain products meet company and regulatory quality standards.&middot; Conduct inspections of raw materials and finished products.&middot; Test grain moisture levels, foreign matter content, and other quality parameters.&middot; Perform physical, chemical, and microbiological testing on grains.&middot; Identify contamination, spoilage, or quality deviations.&middot; Ensure compliance with food safety regulations and quality assurance protocols.&middot; Monitor grain storage conditions to prevent infestation, mold, or degradation.&middot; Assess and approve suppliers based on quality benchmarks.&middot; Maintain detailed records of quality reports and inspection logs.&middot; Prepare reports on quality performance and suggest improvements.&middot; Assist in audits and certification processes.&middot; Require a degree in Food Science, Agriculture, or a related field.&middot; Preferably 1&ndash;3 years of experience in quality control or grain inspection.&middot; Strong analytical, problem-solving, and documentation skills.&middot; Willingness to work in grain storage and processing environments.Job Type: Full-timeWork Location: In person

Quality Analyst

Search 2345+ Microbiological analyst jobs near you this January. New roles added regularly across leading industries. Apply today.

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