Infotree Global Solutions
Get AI-powered advice on this job and more exclusive features.
The QC Microbiologist is responsible for performing microbiological testing and environmental monitoring activities in support of pharmaceutical manufacturing operations. The role ensures that all work is conducted in compliance with cGMP, SOPs, and regulatory requirements while maintaining high standards of accuracy and documentation.
Key Responsibilities:
Perform microbiological sampling and testing of environmental surfaces, air, and utility systems (e.g., purified water, compressed air, gases, etc.).
Conduct environmental monitoring (EM) in controlled manufacturing areas according to established procedures and schedules.
Execute microbial plate counting, bioburden testing, and endotoxin testing on in-process and finished products.
Maintain and review accurate laboratory documentation in compliance with cGMP, GLP, and SOP requirements.
Participate in laboratory housekeeping, calibration, and inventory management.
Qualifications & Experience:
Bachelor’s Degree in Microbiology, Biology, or a related scientific discipline.
Minimum 1 year of experience in the pharmaceutical or biopharmaceutical industry (QC Microbiology preferred).
Hands-on experience with environmental monitoring, bioburden, endotoxin, and microbial enumeration testing.
Knowledge of cGMP, USP, ISO, and regulatory microbiological standards.
Familiarity with LIMS, EM software systems, or data integrity practices.
Basic understanding of sterility testing and microbial identification methods.
Seniority level Associate
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Infotree Global Solutions by 2x
#J-18808-Ljbffr
The QC Microbiologist is responsible for performing microbiological testing and environmental monitoring activities in support of pharmaceutical manufacturing operations. The role ensures that all work is conducted in compliance with cGMP, SOPs, and regulatory requirements while maintaining high standards of accuracy and documentation.
Key Responsibilities:
Perform microbiological sampling and testing of environmental surfaces, air, and utility systems (e.g., purified water, compressed air, gases, etc.).
Conduct environmental monitoring (EM) in controlled manufacturing areas according to established procedures and schedules.
Execute microbial plate counting, bioburden testing, and endotoxin testing on in-process and finished products.
Maintain and review accurate laboratory documentation in compliance with cGMP, GLP, and SOP requirements.
Participate in laboratory housekeeping, calibration, and inventory management.
Qualifications & Experience:
Bachelor’s Degree in Microbiology, Biology, or a related scientific discipline.
Minimum 1 year of experience in the pharmaceutical or biopharmaceutical industry (QC Microbiology preferred).
Hands-on experience with environmental monitoring, bioburden, endotoxin, and microbial enumeration testing.
Knowledge of cGMP, USP, ISO, and regulatory microbiological standards.
Familiarity with LIMS, EM software systems, or data integrity practices.
Basic understanding of sterility testing and microbial identification methods.
Seniority level Associate
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at Infotree Global Solutions by 2x
#J-18808-Ljbffr