61 Sterility Testing Jobs

To perform temperature monitoring of equipment and micro area. To check the calibration tags or external calibration of instrument. To carryout operation and calibration of instrument and maintain usage record. To prepare and maintain records of media preparation, sterilization and disposal. To perform water sampling and testing as suggested in SOP. To perform the Bacterial Endotoxin Test as per SOP. To carryout microbiological testing of raw materials, finished product, hold time study sample, stability samples and packing material. To carryout microbiological testing of cleaning validation samples (swab and rinse). To perform and maintain record of environmental monitoring of controlled areas by settle plate method and air sampler. To maintain and preserve microbial cultures. To enter all the analysis details in job allocation register. To arrange SOP training as per monthly schedule. To monitor the activity and ensure its compliance as per SOP. To check microbiological documents. To carryout qualification of equipment. To adhere to good laboratory practices, good manufacturing practice and good documentation practice. To prepare trends of water analysis and environmental monitoring. To handle the QAMS, DMS, E complain, LIMS, ICDAS Software. To manage all micro related documented activities (Handling of OOS, Lab. Incidence etc.) Immediate joiners will be prefered. Share your resume on dipika.parmar@milanlabs.com

Water testing Sterility Testing BET (LAL) Testing Media Preparation Sub- culturing Environment monitoring Serial dilution GPT testing Micro documentation working Handling of instrument as BOD Incubator Autoclave weighing Balance pH meter TDS meter Microscope

Walk In Drive For Microbiology Department In Formulation Division @ Bollaram Department :- Microbiology Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 5 Years Division :- Formulation Interview Date:-30-07-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-I, Bollaram Venue Location :- MSN Laboratories Pvt Ltd (Formulation Div I) Plot No:-42,Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana-502325. (View on map) Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Role & responsibilities Quality Control: Qualification: B. Pharm/ M. Pharm / M. Sc chemistry Experience: 1 to 6 years of experience in Pharmaceutical Quality Control experience. Job Description: Perform HPLC analysis. Familiarity with analytical laboratory equipment's like HPLC, GC, AAS,ICP-MS, UV, IR and etc., Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniques Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records. Maintain compliance with Current Good Manufacturing Practices in Quality Control and Stability laboratories. Perform testing on various samples, manage Laboratory Information Management System builds. Detail-oriented with robust knowledge of quality control process Effective written and verbal communication, as well as interpersonal skills Experience with Laboratory Information Management Systems (LIMS) Quality Control - Microbiology Qualification: M. Sc(Microbiology) Experience: 1 to 6 years of experience in Pharmaceutical Quality Control - Microbiology. Demonstrated technical skills in microbiology testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, , Bacterial Endotoxin Test, Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Conduct analyses on finished products, raw materials, and components, including data entry, review, Effective written and verbal communication, as well as interpersonal skills

Role & responsibilities To follows cGLP and cGMP in the laboratory. To ensure good housekeeping and maintenance of cleaning record. To execute the microbiological activities and related documentation. To perform the sampling & testing of water (chemical and microbial analysis). To perform the environmental monitoring of the microbiology lab and production area and related documentation. To procure and maintain microbial cultures. To prepare and document disinfectants used for regular cleaning and sanitization of microbiology laboratory. To execute the testing or operating procedure as per current and approved SOPs. To calibrate the Instruments and equipment’s like pH meter, Conductivity meter, Balance etc. To co-ordinate with microbiologist in routine analysis. To Intimate and handle the change control, deviation, out of specification & out of trend. To perform the MLT of raw material, finished product, semi-finished product, stability samples, packing material samples or any other samples. To perform the analytical method validation of the product and related documentation. To perform the Bio Assay & preservative efficacy test and related documentation. To maintain and review the documents and log books which are used in routine analysis. To prepare and standardize volumetric solutions, reagents and indicators. To perform the work given by head microbiologist. To ensure the implementation and compliance with GMP aspects as trained on. To uphold the requirements of data integrity in all activities performed and monitored. To ensure compliance with integrity of data as trained on.

Job Title: Microbiologist Experience: 01 - 03 Years Salary: 2 3.5 LPA Location: Gallops Industrial Park 2, Vasna Chacharvadi, Ahmedabad Job Summary: We are seeking a skilled and detail-oriented Microbiologist with 1 to 3 years of experience to join our quality and laboratory team. The ideal candidate will be responsible for conducting microbiological testing, ensuring compliance with industry standards, and maintaining proper documentation as per regulatory norms. Key Responsibilities: Conduct microbiological analysis of raw materials, in-process samples, and finished products. Perform environmental monitoring and hygiene audits within the production facility. Identify and isolate microorganisms using various culture techniques and instruments. Maintain and calibrate microbiology lab equipment as per SOPs. Prepare and maintain accurate test reports and lab records. Ensure compliance with GMP, GLP, and safety protocols. Coordinate with Quality Assurance/Quality Control and production teams on microbiological issues. Participate in internal audits and assist in regulatory inspections. Ensure proper storage, handling, and disposal of microbial cultures and biohazard materials. Desired Candidate Profile: Bachelor’s or Master’s degree in Microbiology or related life sciences. 1 to 3 years of relevant industrial experience in a microbiology laboratory (pharma/food/cosmetics preferred). Work Location: Gallops Industrial Park 2, Vasna Chacharvadi, Ahmedabad

Eurofins is a leading provider of assurance and inspection services, covering a broad spectrum of sustainable supply chain practices, including the circular economy. Eurofins helps the customers to identify and mitigate risks in their supply chain and to ensure the benchmarking performance with operations, processes, systems, people, or capabilities. We hold accreditations for various industry standards and memberships, ensuring comprehensive service throughout the supply chain. Whether you are in the food, consumer products, healthcare, or cosmetics industries, we offer a full range of services including product inspection, auditing, certification, training, and consultation. Eurofins Assurance helps you mitigate compliance risks, enhance quality, and prevent safety failures early on, safeguarding your business from brand damage, product recalls, and other potential issues in the future. Sustain your business growth and commitment with Eurofins Assurance, a global network of assurance experts that you can trust. Manage accreditation activities. Oversee certification operations. Handle unannounced, semi-announced, and additional audits. Support the Coordinator for reviewing and accepting applications. Maintain auditor qualifications and plan related activities for all schemes. Provide technical support to the team. Address technical queries from clients. Compile scheme updates for clients. Act as the product owner of IT tools for operation management. Verify and submit all scheme data internally and externally (scheme owner and accreditation body). Ensure readiness and updates for dTrackit, eTrackit, GTB, and the BCI portal. Investigate complaints. Conduct technical reviews of audit reports and documentation. Make certification decisions. Conduct calibration, harmonization, and technical training sessions. Manage accreditation activities. Oversee certification operations. Handle unannounced, semi-announced, and additional audits. Support the Coordinator for reviewing and accepting applications. Maintain auditor qualifications and plan related activities for all schemes. Provide technical support to the team. Address technical queries from clients. Compile scheme updates for clients. Act as the product owner of IT tools for operation management. Verify and submit all scheme data internally and externally (scheme owner and accreditation body). Ensure readiness and updates for dTrackit, eTrackit, GTB, and the BCI portal. Investigate complaints. Conduct technical reviews of audit reports and documentation. Make certification decisions. Conduct calibration, harmonization, and technical training sessions. Qualifications Bachelor's Degree in Textile Engineering from a reputed institute (preference for Postgraduates). 12 years of professional experience in a technical capacity in the textile industry, with at least 6 years in a certification body. ISO 9001 Lead Auditor Training Course. ISO 14001 Lead Auditor Training Course. SA 8000 Auditor Training Course. High level of proficiency with standards, related documents, interpretations, and the latest updates. Detailed knowledge of norm requirements for GOTS, GRS, RCS, OCS, MMS, Better Cotton. Knowledge of production methods and processes applicable to textile, plastic, paper, leather, and metal industries. Ability to produce clear, accurate, and complete written audit reports and technical review reports. Experience conducting shadow audits for auditors. Bachelor's Degree in Textile Engineering from a reputed institute (preference for Postgraduates). 12 years of professional experience in a technical capacity in the textile industry, with at least 6 years in a certification body. ISO 9001 Lead Auditor Training Course. ISO 14001 Lead Auditor Training Course. SA 8000 Auditor Training Course. High level of proficiency with standards, related documents, interpretations, and the latest updates. Detailed knowledge of norm requirements for GOTS, GRS, RCS, OCS, MMS, Better Cotton. Knowledge of production methods and processes applicable to textile, plastic, paper, leather, and metal industries. Ability to produce clear, accurate, and complete written audit reports and technical review reports. Experience conducting shadow audits for auditors. Additional Information Impeccable proficiency in both written and spoken English. Knowledge of a foreign language is an added advantage. Highly organized with the ability to plan and prioritize work. Efficient time management. Working knowledge of Microsoft Office tools (Word, Excel, PowerPoint, SharePoint, Teams). Experience with IT tools used in certification or accreditation bodies.

1.Preparation of dilute disinfectants and ensure microbiology area cleaning. 2.Temperature, Relative humidity (RH) and Differential pressure (DP) monitoring in Microbiology Laboratory. 3.Sampling of water as per the schedule. 4.Execution of environmental monitoring activities in the microbiology laboratory and manufacturing facility as per the schedule. 5.Receipt, storage and Preparation of Microbiological media followed by growth promotion testing. 6.Gowning qualification of Personnel Involved in Aseptic Operations.

Sterilization and preparation of media, Media growth promotion test, Media fill validations. Analysis of Pathogenesis test, MET, Environmental monitoring. Hands on experience in Analyzing of ELISA techniques like Binding ELISAs, Impurity based Assays HCP, LPA. Analysis of electrophoresis methods such as SDS-PAGE, IEF. Analysis of In-Process, DS, DP and Stability samples. Exractable volume of final DP sample. Aliquoting of batch release, stability samples. Withdrawing of stability samples as per the protocol. Receiving, storage and Physical verification of Reserve samples

1. Receipt, storage and usage of medias, Microbial cultures, materials and documentation 2. Perform viable / non-viable monitoring activities, media plates observations and documentation in testing facilities. 3. Environmental monitoring, sampling, receipt, testing and documentation of all Microbiology samples. 4. Perform cleaning, fumigation and other activities in Microbiology laboratory. 5. Monitoring of temperature, DP and RH of the Microbiology laboratory. 6. Preparation of dilute disinfectants, reagents solutions / indicator solutions. 7. Responsible for compliance to cGLP. 8. Operation and usage of instruments. 9. Execution of method validations / method verification samples. 10. Receipt / testing of validation samples from manufacturing / other areas 11. Training and qualification of analysts in Microbiology department. 12. Responsible for handling of Bio-waste in Microbiology department. 13. Review, checking and verification Microbiology laboratory documents. 14. Responsible for implementation activities related to resource manager and sample manager of Laboratory information management System #40;LIMS#41;

1. Receipt, storage and usage of medias, Microbial cultures, materials and documentation 2. Perform viable / non-viable monitoring activities, media plates observations and documentation in testing facilities. 3. Environmental monitoring, sampling, receipt, testing and documentation of all Microbiology samples. 4. Perform cleaning, fumigation and other activities in Microbiology laboratory. 5. Monitoring of temperature, DP and RH of the Microbiology laboratory. 6. Preparation of dilute disinfectants, reagents solutions / indicator solutions. 7. Responsible for compliance to cGLP. 8. Operation and usage of instruments. 9. Execution of method validations / method verification samples. 10. Receipt / testing of validation samples from manufacturing / other areas 11. Training and qualification of analysts in Microbiology department. 12. Responsible for handling of Bio-waste in Microbiology department. 13. Review, checking and verification Microbiology laboratory documents. 14. Responsible for implementation activities related to resource manager and sample manager of Laboratory information management System #40;LIMS#41;

Role & responsibilities 1. Responsible for Daily sampling and analysis of in-process and water samples as per procedure. 2. Responsible For Preparation and pouring of media plate. 3. To perform BET (Bacterial Endotoxin Test) test and Microassay. 4. To perform Sterility Test, Bioburden and MLT (Microbial Limit Test) or water and product. 5. To Perform Growth Promotion / Inhibitory / Indicative Property Test Of Media. 6. To report results of analysis in raw data sheet issued. 7. Entry and maintain all micro related logbooks. 8. To Follow the QMS (Quality Management System) system (Out of Specification, Deviation, Incident) 9. To participates in validation activity. 10. Observation and review of media fill container. 11. To perform environmental monitoring in clean room as per standard operating procedure. 12. To run the autoclave cycles and unload the loads as per SOP (Standard operation procedure). 13. To monitor incubator condition daily and record, to take print out and verify. 14. To maintain the GLP (Good laboratory practices) and follow GDP (Good documentation practices) in the laboratory. 15. To run washing and drying machine. 16. To raise Out of Specification if noticed. 17. Responsible to perform analysis of Analytical method Validation, Analytical method Transfer, reconstitute Solution stability, additional analytical test required as per party quarry reply. 18. Responsible for preparation Analytical method validation protocol, raw data, report. 19. Responsible for review of Analytical method validation protocol, raw data, report. 20. Responsible for preparation excel sheet preparation of analytical method validation, method transfer, Reconstitute Solution Stability study. 21. Responsible for planning of method validation activity. Requirement of sample, standard, reference standard, column, instrument provide to the analyst. 22. Responsible for training providing to the analyst for analytical method validation and method transfer SOPs (Standard operating procedures). 23. Responsible to control and maintain records like protocols, raw data, and report of method validation, method transfer and reconstitute solution stability. Analysis records, usage log books and status labels during day to day Analysis of validation. 24. Any other Responsibility assigned by HOD (Head of Department). 25. To assist HOD (Head of Department) for the preparation of regulatory inspection. Preferred candidate profile Candidate Should be From Pharma Background Good Verbal and Written Communication Willing to Relocate in Navsari , Gujarat Willing to Work in a Shift

Intersted candidates can send their CVs on career@scott-edil.com or can contact on 9805091898 We are seeking a dynamic and experienced Micro QC- Offcer/ Sr. Offcer/ Executive /Sr. Executive to join our Quality Control team. The ideal candidate will have 2 to 6 years of hands-on experience in microbiological quality control, with strong exposure to both Oral Solid Dosage (OSD) and Injectable formulations. The candidate must have practical knowledge of Environmental Monitoring (EM) and a solid understanding of GMP/GLP practices in a regulated manufacturing environment. Role & responsibilities Preferred candidate profile Perform routine microbiological testing of raw materials, finished products, and in-process samples. Conduct Environmental Monitoring (EM) in cleanrooms, including air sampling, surface sampling, and personnel monitoring. Handle microbial limit testing, sterility testing, BET, and water analysis. Manage and review microbiological documentation and records as per regulatory guidelines. Support validation activities for cleanroom qualification and water systems. Investigate and document any non-conformances or deviations. Coordinate with cross-functional teams including production, QA, and engineering for EM-related observations and improvements. Ensure compliance with cGMP, regulatory standards, and company SOPs.

Dear Candidate , we are hiring for Biologics for the Position JR Executive . Bio burden testing of in process samples as per the specification. BET testing of water samples, in-process samples, semi-finished and finished samples as per the specification. Sterility testing of finished product. Responsible to perform the MLT testing for raw materials and water samples. Maintenance and handling of Endotoxin indicators and biological indicators. Experience on culture maintenance and VITEK2 compact system To perform the method validations for MLT, BET, Bio burden and Sterility. Injectables or biologics experience is mandatory. Male candidates are preferable. Regulatory audits exposure is mandatory. Department:- Microbiology . Exp:-2-5 Years. Des:- Jr Executive-Executive . Qua:-MSc Microbiology . NOTE : Only Male Candidates Preferable for more details please reach out Venkat -9381915043 or please share your CV to venkateswara.k@talent21.in

JD Of Microbiologist Job Title: Microbiologist Experience 3-5 years Location: Kala Amb Job Summary: We are seeking a motivated Microbiologist with xperience to conduct microbiological testing, analyze results, and support laboratory operations. The ideal candidate will have hands-on experience in microbial culture techniques, sterility testing, and environmental monitoring. Key Responsibilities: Perform microbiological testing on raw materials, in-process samples, and finished products Conduct environmental monitoring and sterility assurance Isolate and identify microorganisms using standard microbiological methods Maintain accurate laboratory records and ensure compliance

1. Microbial Testing MLT and Pathogens 2. Environmental Monitoring- Clean room viable and non-viable particle counts 3. Water Testing - specific pathogens. 4. Documentation and reporting as per GDP

Responsibilities: Bioburden Testing BET & Sterility Testing Handling of Endotoxin Indicators & Biological Indicators. Culture maintenance Vitek2 Compact System handling Regulatory Audit exposure Injectable or Biological Experience is Mandatory

Dear Candidate , we are hiring for Fresher for the position Microbiologist . Job Description: Department:- Microbiology Exp: 2.0 yrs to 3.0 yrs Des:- Jr Executive-Executive Qua:-MSc Microbiology Only Male Candidates Preferable Bio burden testing of in process samples as per the specification. BET testing of water samples, in-process samples, semi-finished and finished samples as per the specification. Sterility testing of finished product. Responsible to perform the MLT testing for raw materials and water samples. Maintenance and handling of Endotoxin indicators and biological indicators. Experience on culture maintenance and VITEK2 compact system To perform the method validations for MLT, BET, Bio burden and Sterility. Injectables or biologics experience is mandatory. Male candidates are preferable. Regulatory audits exposure is mandatory. IMMEDIATE JOINERS ARE PREFERABLE"

Perform routine Environmental Monitoring activities: viable and non-viable monitoring, surface monitoring, personnel monitoring. Good knowledge of cleanroom classification (ISO 14644), Good Manufacting P and EM requirements Ability to prepare and execute validation protocols and summarize reports Skilled in microbial monitoring techniques and aseptic area behaviour. Strong documentation, audit readiness, and data integrity practices

Responsibilities: * Conduct microbiological testing on water samples using MLT, BET & MLR methods. * Perform environmental monitoring and sterility testing.

The CSSD Technician is responsible for the effective sterilization and disinfection of surgical instruments and medical equipment. This role involves preparing, sterilizing, and ensuring the safe handling of instruments to maintain the highest standards of hygiene and safety within the hospital environment. The technician will also be responsible for the quality control of sterilization processes and will work closely with various departments to support surgical procedures. Roles and Responsibilities - Clean, decontaminate, and sterilize instruments and medical equipment using appropriate methods and technologies. - Ensure the proper functioning of sterilization equipment and report any malfunctions. - Monitor and maintain sterilization logs and quality assurance records. - Prepare and package instruments for surgery, following established protocols. - Collaborate with surgical teams to meet instrument and equipment needs during procedures. - Follow infection control standards and safety protocols to prevent contamination. - Conduct routine checks and maintenance of CSSD supplies and inventory management. - Participate in ongoing training and professional development related to sterilization techniques and infection control practices. Skills Required: - Knowledge of sterilization techniques, principles of infection control, and safety standards. - Familiarity with surgical instruments and medical equipment. - Attention to detail and strong organizational skills. - Ability to work under pressure and manage time effectively. - Excellent communication and teamwork skills. - Analytical skills to monitor sterilization processes and troubleshoot issues. Tools and Equipment: - Autoclaves and sterilization equipment. - Decontamination tools and instruments. - Personal protective equipment (PPE). - Inventory management software. - Quality control systems and logging tools.

Sterility, bioburden, endotoxin, AET/PET testing Method validation for medical & polymer products Lab setup, media prep, equipment handling Water (WFI/CS) & environmental monitoring Data review as per cGMP & compliance norms and Maintain lab records

Job Title: Research Assistant Quality Control (QC) Department: Quality Control Location: Noida Company: Advancells Group Salary Range: 25,000 - 40,000 per month Preference : Male Candidate, Immediate Joiner About Advancells Group: Advancells is a pioneering leader in stem cell manufacturing and regenerative medicine. Our mission is to bring cutting-edge biomedical science into practical application for patient well-being and healthcare innovation. As part of our growth, we are hiring passionate professionals to join our Quality Control team. Role Overview: We are looking for a committed and detail-oriented Research Assistant QC to support on-site quality control operations, microbiological testing, and packaging inspection activities. The role will involve hands-on testing, documentation, and collaboration with the production team to uphold product quality and GMP compliance. Key Responsibilities: Perform microbiological testing on raw materials, in-process samples, and finished goods. Conduct Sterility Testing and Bacterial Endotoxin Testing (BET) as per pharmacopeial and SOP standards. Execute and record Quality Control checks for product packaging and labeling. Support in-process quality checks on production floor to ensure hygiene and GMP adherence. Conduct visual and physical inspections for finished product quality parameters. Perform routine environmental monitoring , cleanroom checks, and personnel hygiene audits. Assist in line clearance activities before and after batch production. Participate in root cause analysis of non-conformities, especially related to packaging or contamination issues. Ensure Good Documentation Practices (GDP) while recording observations and test results. Be available for on-site physical tasks such as sampling, validations, and quality checks during production. Support field activities such as transporting samples, overseeing external testing, and maintaining sample integrity. Candidate Requirements: Qualification: M.Sc. in Microbiology / Biotechnology / Life Sciences (preferred) Experience: 13 years in QC/QA roles within pharmaceutical, biotech, or stem cell environments. Strong understanding of GMP, GDP, and QC protocols . Hands-on experience in microbiological testing and working in cleanroom environments . Good interpersonal skills and ability to coordinate with production and documentation teams. Immediate joiners will be given preference. Why Join Us? Be part of India's leading organization in regenerative medicine. Work in a GMP-certified lab environment with world-class QC standards. Growth opportunities in a fast-evolving biomedical industry. How to Apply: Send your updated resume to hr@advancells.com with the subject line: Application for Research Assistant QC . Immediate joiners will be prioritized.

Position: Executive (Microbiology) Qualification: M.Sc (Microbiology) Experience: 3-8 Years Location: Torrent R&D Centre, Gandhinagar, Gujarat Requirement: Strong knowledge in planning and execution of microbial activities like BET/Endotoxin/Lysate sensitivity test , sterility , GPT, PET, MLT /Bioburden/ specified microorganisms method development and validation for finish product, raw material, in-process samples etc. Expertise in operation and validation/calibration of microbiology lab related instruments. Knowledge of handling of Trackwise and QMS activities. Able to develop and validate the method for antibiotic assays for different dosage forms . Strong knowledge in microbial pathways and probiotic characterization (from sample preparation to data analysis to results interpretations).

Role & responsibilities To perform the microbial limit test & validation of samples as per GLP and other different types of samples. To perform Sterility test, BET test & Preservative Efficacy testing of different samples & to perform their validation activity. To monitor the environment of the Microbiology lab. To perform the sterilization of glassware's by autoclave and dry heat sterilizer. To prepare the microbiological media and chemical reagent as and when required and perform the necessary microbial tests. Preparation of disinfectant solution Daily, quarterly and yearly calibration of the balance, pH meter and other instruments as per the master schedule. To check the performance of all instruments as per the master schedule. To review the microbiological documents. To approve the microbiological test related TRF. Documentation and writing journals related to the microbiological test and there validation. To represent the Microbiological lab during audits . Preferred candidate profile M.Sc (Micro) with 02-07 Yrs of relent experience. Interested Candidate may share their Cvs on vilshashah@torrentpharma.com