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5.0 - 9.0 years
0 Lacs
punjab
On-site
The job involves ensuring microbiological work in compliance with GLP and Regulatory lab standards. This includes tasks such as media preparation, GPT Test, Bioburden Test, MLT, Microbial Assay, Efficacy Test, AMV Test, Sterility Test, Bacterial Endotoxin Test (BET), Environmental Monitoring test, Swab Analysis, Culture and Maintenance, GPT Record, Pathogen Analysis, Grams Staining technique, and calibration of all instruments related to the Micro Lab. Additionally, the role requires QC labeling of all documentation related to the Microbiology Lab according to GLP, GMP, WHO & EU GMP guidelines. The position is full-time and permanent, with benefits including Provident Fund. The work schedule involves day and morning shifts, and the ideal candidate should have a total of 5 years of work experience. The work location is in person.,
Posted 3 weeks ago
3.0 - 7.0 years
0 Lacs
vadodara, gujarat
On-site
As a part of this role, you will be responsible for method development, method validation, and routine analysis in Orals and Non-orals Formulations. Your area of experience will include conducting the Microbial Enumeration Test, Test for specified Micro-organisms, Bio-burden Test, Antimicrobial Effectiveness Test, Sterility Test, Bacterial Endotoxin Test, Microbiological Assay, Microbial Culture propagation, maintenance, and enumeration, Growth Promotion Test, as well as Environment monitoring. In addition to the above, you will also be involved in the preparation of SOP's/STP's/Documentation, calibration of laboratory equipment/Instrument, ensuring work is conducted as per cGMP/GLP Compliance, and having exposure to LIMS. Your role is crucial in ensuring the accuracy and reliability of testing procedures and results, and your expertise in various microbiological tests will contribute significantly to the overall quality and compliance standards of the organization.,
Posted 1 month ago
3.0 - 8.0 years
3 - 8 Lacs
Sonipat
Work from Office
Microbiological testing, monitoring & sterility assurance, Initiate CAPA, Generate & execute microbial method validation protocols/report, Microbiology procedures, validations, records including writing, routing, approval for Medical Device Industry. Required Candidate profile BSc/ MSc in Microbiology with 3+ year exp. as a Microbiologist in a medical device company. Hands-on with microbiology standards including AAMI ST72, ISO 11737, ISO 14644, ISO 11137, ISO 11135, USP.
Posted 2 months ago
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