Research Assistant

Integrated Resources, Inc ( IRI ); Memphis (TN); On-site; USD 45,000 - 65,000; Full time

Job summary

Integrated Resources, Inc in Memphis, TN seeks a Quality Control Analyst I to support the QC Microbiology Department. The role focuses on environmental monitoring, product-release testing, and raw material testing with attention to detail and strong organizational skills.

Responsibilities include sample processing, inventory management, SOP compliance, and data integrity across GMP systems. Effective communication and ability to work in a fast-paced, technical environment are essential.

Qualifications

• Attention to detail required for accurate sample processing and data recording.
• Strong organizational skills to manage samples, logs and inventory.
• Proficiency with computer systems for data entry, documentation and reporting.
• Fundamental microbiology understanding and lab instrumentation familiarity.

Responsibilities

• Performs environmental monitoring including air viable and non-viable particulate sampling and surface sampling.
• Receives materials for QC lab and maintains supplies, media and reagents inventory.
• Adheres to SOPs and good documentation practices to ensure data integrity and traceability.
• Maintains operation of the department through logs, filing and organization.

Skills

Attention to detail

Organizational skills

Computer proficiency

Microbiology knowledge

Tools

MODA

Job description

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.