165 Sterility Testing Jobs

Perform Environmental Monitoring in classified area, Monitor compressed air, gases, utilities as per SOP, Ensure documentation as per cGMP & ALCOA+ principles, understanding of microbiological techniques streaking, aseptic technique, culture handling

SOP, GTP, protocol Preparation Instrument calibration Review all document OOS/Incident/Deviation Preparation Training Activity Media as well as required item management Calibration schedule preparation Water Analysis, Water Testing, Media Preparation, Sterility Testing, Environmental Monitoring,

Perform microbiological testing of RM, intermediates, FP & water. Conduct EM, MLT, sterility, endotoxin & bioburden tests. Handle method validation, media prep, equipment qualification, documentation, deviations & ensure cGMP and DI compliance.

Role & responsibilities * Bio burden testing of in process samples as per the BET testing of water samples, in-process samples, semi-finished and finished samples as per the specification. * Sterility testing of finished product. water samples. * Maintenance and handling of Endotoxin indicators and biological indicators. * Experience on culture maintenance and VITEK2 compact system and Sterility. • Injectables or biologics experience is mandatory. * Regulatory audits exposure is mandatory.

Responsible to prepare protocols ,reports, Sop's, review docs and analysis, methods development, verification validations for AET,MLT Sterility test& BET, follow GMP&GLP,SILUTION STUDY/microbial ingress study.

About company: Eris Lifesciences Ltd. is a publicly listed Indian pharmaceutical company and ranks among the Top-20 companies in the Indian formulations industry. Founded in the year 2017, it is the youngest company to feature among the Top-20. With consolidated revenue in excess of USD 340 million, Eris has grown over 5x in the last 10 years. The company has a market capitalization of ~ USD 3 billion and ranks among the fastest growing and most profitable pharmaceutical companies in India. Swiss Parenterals Limited is a subsidiary of Eris and has a successful 25-years plus legacy of manufacturing the widest range of sterile injectable formulations in its two manufacturing units in Gujarat. ...

Walk In Drive For Microbiology Department In Formulation Division @ Jadcherla Department:- Microbiology Qualification :-BSC Microbiology | MSC Microbiology Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in MLT, BET, Media Preparation,EM, Sterility Test. About Company:- MSN Group is the fastest growing research-based ph...

Role Overview: As a QC Microbiology Reviewer at Syngene, you will be responsible for conducting microbiological analysis, sterility testing, bacterial endotoxin tests, and analyzing different grades of water according to specifications. Your role will involve preparing risk assessment documents, protocols, and reports, as well as managing the Quality Management System (QMS) related to microbiology. Additionally, you will oversee area qualifications, calibrations, equipment qualifications, and sample management activities to ensure the smooth operation of the microbiology laboratory. Key Responsibilities: - Conduct microbiological analysis, sterility testing, and various microbiology tests - ...

Responsibilities: 1. Conduct environmental monitoring, microbial testing, sterilization processes. 2. Prepare media, perform water analysis, document audits and compliance. 3. QMS, cGMP, GLP practices. Training, Investigation and troubleshooting Health insurance Provident fund

Role & responsibilities Perform sterility testing and microbiological analysis of RM, intermediates, stability, and finished products. Follow SOPs and report any OOS results or deviations to Head QC. Monitor classified areas and enter environmental data for trend analysis . Ensure proper area cleaning, gowning, and instrument maintenance as per cGMP. Coordinate material flow, including receipt and distribution for analysis. Follow EHS policies and ensure safe use of PPE. Support and mentor team members, allocate tasks, and maintain high employee engagement . Interested candidate kindly send your updated resume to mounika@bvrpc.com

Title: Head - Microbiology Business Unit: SGO Quality Job Grade Senior Manager Location: Mohali Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” JOB DESCRIPTION Responsible for Oversight and M...

Walk In Drive For Microbiology Department In Formulation Division @ Kothur Department :- Microbiology Qualification :- BSC | MSC - (Microbiology| Biotechnology | Biochemistry ) Experience :- 2 to 8 Years Division :- Formulation Interview Date:-29 -11-2025 Interview Time:- 9.00AM TO 2.00PM Work Location :- MSNF-II, Kothur,MSNF-V R.K.Puram Venue Location:- MSNF-II, Kothur Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Note:- Candidate should bring Update Resume , Certificates, Aadhaar 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 ma...

Job Description: Formulation & Development Sterile Department: Formulation & Development Location: Rabale Key Responsibilities: 1. Sterile Formulation Development Develop formulations for sterile dosage forms such as injectable solutions, suspensions, emulsions, lyophilized products, and ophthalmics. Execute pre-formulation studies, compatibility studies, and stability studies. Optimize formulas and processes to meet product quality, safety, and regulatory standards. 2. Aseptic Manufacturing Support Work closely with production during scaling-up and pilot/batch manufacturing in aseptic areas. Ensure adherence to aseptic processing guidelines and cleanroom behavior practices. 3. Process Devel...

A microbiologist studies microorganisms like bacteria, viruses, and fungi to conduct research, analyze samples, and develop solutions for various challenges in healthcare, industry, and the environment . Key responsibilities include performing lab tests, isolating and identifying microbes, ensuring safety protocols, and documenting findings, while skills like analytical thinking and attention to detail are essential. Core duties and responsibilities Conduct research and experiments: Study the life processes and effects of microorganisms on humans, animals, plants, and the environment. Perform laboratory analysis: Test samples (clinical, food, water, pharmaceutical) for contamination, infecti...

Role & responsibilities To ensure the clean environment for sterile preparation by implementing the Good Manufacturing Practice (GMP) norms as per the international standards and guidelines. To do sampling of Water for Injection (WFI), Double Reverse Osmosis (DRO), Single Reverse Osmosis (SRO), Raw water and pure steam. To analyze water samples for pH, conductivity, Bacterial Endotoxin Test (BET), bioburden, Total Organic Carbon (TOC), pathogens, chlorides, hardness, silt density index and other testing as per the requirements. To analyze the samples of water system after maintenance work . To observe and record the results the microbiological plates and test tubes after analysis as well as ...

Open Positions Microbiology (0 to 6 Years) (Qualification: M.Sc-Microbiology/Biotechnology) Experience in Disinfectant Preparation, Media Preparation, MLT, BET, Sterility Testing, Method Validation & Documentation Experience in Culture Handling and Environmental Monitoring Engineering (2 to 6 Years) (Qualification: ITI / Diploma / B.Tech) Hands-on experience in operating Lyophilizers Experience in Water System & HVAC operations Experience in Instrumentation activities Production (0 to 10 Years) (Qualification: ITI / Diploma / B.Sc / B.Pharm / M.Pharm) Skilled in operation and supervision of filling lines Ability to supervise packing lines Strong expertise in Production QMS Training supervisi...

As a **Manufacturing and Microbiology Technician**, you will be responsible for participating in performing qualification activities in the manufacturing and Microbiology area. Your key responsibilities will include: - Monitoring compressed air and nitrogen gas, as well as personnel monitoring. - Planning and executing environmental monitoring of manufacturing and microbiology lab clean room areas according to defined schedules. - Planning compressed air and nitrogen gas monitoring, and personnel monitoring activities. - Performing calibration and qualification of instruments and equipment as per the predefined schedule. - Participating in media fill simulation studies. - Handling sterility ...

Officer - Microbiologist: Qualification M.Sc (Micrbiology) / B. Pharm / M. Pharm Experience 02 - 04 yrs in microbiological testing in pharmaceutical industry Job Description To prepare media, sterilize and conductgrowth promotion test. To perform sampling & analysis of purified & potable water for chemical & microbiological testing. To perform microbiological analysis offinished goods and raw material.(MLT & Microbiological Assay) Handling of microbial cultures and itsmaintenance. To receipt Media, do labelling andmaintain stock record. To handle instrument and performcalibration. Bio burden testing of packaging material. Maintain logbooks and related records. Ensure GLP Compliance.

Responsible for managing and setting the direction of the QC Laboratory operations (Microbiology) in a Sterile cGMP environment. Main responsibility is to assure the reliability of all data generated by the Quality Control Laboratory, and provide support for the Sites environmental monitoring program. Major Responsibilities: Supervision, training and development of reporting QC Microbiology staff, and provide guidance on best aseptic practices for all aseptic (Sterile) area personnel. Management of the Environmental Program, as backup to the Site Microbiologist. Trend analysis and evaluation of critical system data; this may include environmental monitoring reports. Management adherence to t...

Role & responsibilities Environment monitoring of QC and production area. To prepare Trends of Environment monitoring and water testing. Sterility Test, sterility test observation and sterility test method validation. Establishing procedures for Microbiological testing, Documents review. Preparation of all microbiology documentation, training and effectiveness of documents. Microbial testing of Water, Bioburden, Raw material, Bulk samples its release & documentation. Maintaining Good Laboratory Practices throughout the Quality Control laboratory and good documentation practices Checking of daily release sterility test tubes & documentation. Bacterial Endotoxin Testing, method validation & it...

Job Title: Senior Microbiology Trainer Location: Remote Job type: Part-time Job Summary: We are seeking a highly experienced Microbiology Trainer with over 10 years of professional experience in academic, industrial, or laboratory microbiology. The trainer will design, deliver, and evaluate microbiology training programs for students, fresh graduates, and professionals working in pharmaceutical, food, and life sciences industries. Key Responsibilities: Conduct hands-on and theoretical training sessions on Microbiology fundamentals , Industrial & Pharmaceutical Microbiology , and Quality Control techniques . Train participants on GMP/GLP , sterility testing , environmental monitoring , microb...

Role & responsibilities - Responsible for driving excellence in sterility assurance practices, meeting the global regulatory requirements, drive sterility Assurance Program at site - Conduct sterile quality management review periodically - Periodic review and routine check of classified areas like manufacturing, Microbiology and utility areas - Preparation & adherence to Sterility Assurance Calendar consisting of Review timelines, training calendar and requalification - Ensuring SOP adherence to clean room facility / utilities/ equipment / Personnel qualifications whichever has a potential to impact the Sterility of the product. - Review validation / protocol studies which has potential to d...

Role & responsibilities: Environmental monitoring of microbiology laboratory and production area as per schedule. Monitoring of temperature, humidity and differential pressure of microbiology laboratory To receive, prepare, sterilize and usage the microbiological media as per standard operating procedure. MLT Test of RM, FP, Bulk, Packing material as per pharmacopeia Sampling of treated water, purified water and R.O water as per specified schedule. Microbiological analysis of treated water and purified water as per standard operating procedure. Sterility test, BET Test, media Fill, BIs test Area validation and qualification. Validation of autoclave, Incubators & Dry heat sterilizer. Online D...

As an In charge of the Microbiology Department in the pharmaceutical industry with 5+ years of experience, your role involves performing microbiological testing of raw materials, in-process samples, finished products, and environmental samples to ensure compliance with GMP and regulatory standards. Key Responsibilities: - Perform microbiological analysis of raw materials, in-process samples, and finished products. - Conduct environmental monitoring of production and microbiology areas (air, surface, personnel monitoring, etc.). - Perform tests such as Sterility Testing, Endotoxin Testing (LAL test), Microbial Limit Test (MLT), and Water Testing (RO, Purified, WFI). - Prepare and maintain cul...

As a Quality Control Testing Technician in a Cell Therapy Lab, your primary responsibility is to ensure the quality and safety of cell therapy products through rigorous testing and analysis. You will work in a highly regulated environment, adhering to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to support the development and production of cell-based therapies. This role requires a strong attention to detail, analytical skills, and the ability to work collaboratively with cross-functional teams. - Execute a variety of tests to assess the quality, purity, and potency of cell therapy products, including but not limited to viability assays, sterility testing, endotoxin...