Schedule: Sun-Thu 2pm-11pm POSITION SUMMARY The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material testing. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Performs environmental monitoring, including air viable particulate, non-viable particulate and surface sampling and personnel monitoring * Receives raw materials and supplies for the QC laboratory and maintains laboratory supplies, media and reagents inventory * Adheres to standard operating procedures and good documentation practices to ensure data integrity and traceability * Participates with maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.) * Responsible for assisting with routine laboratory upkeep and organization * Utilizes GMP systems such as MODA and other laboratory computer systems * Reviews test results of other QC analysts for accuracy and precision and maintains and efficient workflow of all required testing documentation ensuring timely submission relative to product release dates * Perform all other related duties as assigned. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Performs sterility testing and endotoxin testing of raw materials, in-process samples and finished products * Performs growth promotion of microbial media * Performs environmental monitoring, including air viable particulate, non-viable particulate and surface sampling and personnel monitoring * Prepares environmental monitoring excursion reports and conducts minor laboratory investigations. * Receives raw materials and supplies for the QC laboratory and maintains laboratory supplies, media and reagents inventory * Adheres to standard operating procedures and good documentation practices to ensure data integrity and traceability * Assists the QC Supervisor/Leads with managing proper overall operation of department (physical inventories, logs, documentation, filing, etc.) * Maintains familiarity with QC-relevant current Good Manufacturing Practices (cGMP) guidance (CFR, USP, EP, ICH, etc.) * Responsible for assisting with routine laboratory upkeep and organization * Reviews test results of other QC analysts for accuracy and precision and maintains and efficient workflow of all required testing documentation ensuring timely submission relative to product release dates * Perform other related duties as assigned QUALIFICATIONS: * Bachelor’s degree in biology or relevant scientific discipline required * Minimum 0-2 years relevant laboratory experience or experience in a cGMP and/or FDA regulated industry or a combination of education and related work experience required * May consider less education and professional experience upon successful completion of the companies internship program * Ability to work in Clean Room environment with full gowning requirements * Ability to work independently or as a team member * Detail-oriented with strong written and verbal communication skills * Demonstrated knowledge in Microbiology and aseptic techniques * Ability to problem-solve and troubleshoot as necessary * Familiarity with laser particle counters, viable air samplers, microscope, Endosafe® Instrumentation, PCR, BacT/ALERT systems The max pay rate is 21.13/hr for this position