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0.0 - 2.0 years
1 - 3 Lacs
Hyderabad
Work from Office
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.
Posted 4 days ago
3.0 - 4.0 years
1 - 4 Lacs
Hyderabad
Work from Office
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
Posted 4 days ago
3.0 - 8.0 years
4 - 9 Lacs
Gandhinagar
Work from Office
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).
Posted 3 weeks ago
5.0 - 10.0 years
4 - 9 Lacs
Hyderabad
Work from Office
Role & responsibilities To follow the cGMP, Safety norms and adhere to company's policy. Performing Microbial Limit Test for Non-Sterile Products (API's), Validations, Verifications and Method developments BET analysis for water and Pharmaceutical products. Operation and handling of Instruments/Equipment's. Preparation of work sheets, SOP/GTP's and STP's for Microbiology Laboratory. Assessment of test results against specifications and Trend data. Checking of inwards registers, equipment log books and other log books for all entries. Handling of OOS and Deviations and Incidents. Attending Training classes like OJT, cGMP, SOP, External and safety programs as per schedule. Conducting Training classes like cGMP, OJT, SOP and safety programs as per schedule. Environmental Monitoring by Active and Passive air sampling methods in clean rooms and Microbiology Lab. Carryout Cleaning and Calibration of laboratory Instruments and Equipment's. Media preparation, sterilization and Growth Promotion Test of media.
Posted 1 month ago
3.0 - 6.0 years
5 - 9 Lacs
Bengaluru
Work from Office
Backup Administration, Macro/Micro Segmentation, IOT Security Expertise in VLAN segmentation, IT/OT isolation strategies, and backup management Strong project management skills for implementing security measures across multiple sites Excellent communication skills for stakeholder engagement and leadership reporting Analytical mindset for identifying risks and designing effective mitigation strategies
Posted 1 month ago
3.0 - 8.0 years
4 - 7 Lacs
Gangtok, Rangpo
Work from Office
To prepare, review and approve Quality Control-Microbiology Documents-Study Protocol, General Test Procedure, Specifications, Qualification Protocols. To perform and review daily Verification, Calibration of Quality Control-Microbiology instruments. To prepare and review the Trend data of Water and Environment Monitoring. To perform sampling, analysis & observation of water and recording relevant data. To perform and review Microbiological Limit Test/Method suitability testing of raw material, in-process and finished products. Preparation and review of culture media and performance of growth promotion test of media. To review the Microbiology reports and documentation. Preferred candidate profile 5 - 6 yrs of experience in Microbiology M Sc in Microbiology or Biotechnology Interested candidates may share profile at hr.plant@zuventus.com
Posted 1 month ago
10.0 - 15.0 years
10 - 18 Lacs
Baddi
Work from Office
Role & responsibilities Key Responsibilities: Lead the Microbiology Laboratory operations for injectable manufacturing in accordance with cGMP and global regulatory guidelines. Oversee and ensure compliance in microbiological testing such as: Sterility Testing Bacterial Endotoxin Testing (LAL) Environmental and Personnel Monitoring Bioburden and Microbial Limit Tests (MLT) Water and utility microbiological assessments (WFI, purified water, compressed air) Design, execute, and review microbiological method validation protocols including: Validation of Sterility Test methods BET (LAL) method suitability and validation Disinfectant efficacy studies Antimicrobial effectiveness testing Microbial recovery studies from various matrices and surfaces Lead cleanroom validations, aseptic process simulations (Media Fills), and HVAC system qualification from microbiological perspective. Serve as subject matter expert (SME) during inspections (EU, PICS, COFEPRIS, WHO-GMP, etc.) and customer audits. Drive root cause analysis (RCA), CAPA implementation, and continual improvement related to microbial excursions or contamination events. Maintain and periodically update SOPs, microbiological risk assessments, and QMS documents. Develop and mentor a team of qualified microbiologists. Coordinate with QA, Production, and Validation teams for cross-functional initiatives and technology transfers. Preferred candidate profile M.Sc. in Microbiology or related field. 1215 years of relevant experience in a sterile pharmaceutical environment with a strong background in injectables . Hands-on expertise in microbiological method validations and regulatory-compliant documentation practices. Proven track record of successful regulatory audits and inspections. Strong grasp of current regulatory guidelines: USP, EP, JP, ICH, WHO TRS , etc. Familiarity with laboratory instrumentation like isolators, automated endotoxin readers, particle counters, and bio-safety cabinets. Desired Competencies: Strong leadership and decision-making skills. Meticulous attention to detail and scientific integrity. Effective communication and team-building abilities. High level of regulatory awareness and industry best practices.
Posted 1 month ago
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