QC Analyst I-Microbiology

Planet Pharma; Memphis (TN); On-site; USD 24,000 - 34,000; Full time

Job summary

Planet Pharma is seeking a Quality Control Analyst I for the QC Microbiology Department in Memphis. The role involves processing routine environmental monitoring samples, product-release testing, and raw material testing with attention to detail and strong communication in a fast-paced lab.

The position requires basic microbiology knowledge, aseptic techniques, and ability to work in a clean room. Experience with GMP systems and lab instrumentation is a plus.

Qualifications

• Bachelor's degree in biology or relevant scientific discipline is required.
• 0-2 years of relevant laboratory experience or FDA/cGMP exposure preferred.
• Able to work in a Clean Room with full gowning requirements.
• Strong written and verbal communication; detail-oriented work.
• Familiarity with microbiology techniques and aseptic handling.

Responsibilities

• Perform environmental monitoring including air and surface sampling and personnel monitoring.
• Receive and inventory laboratory supplies, media and reagents.
• Adhere to SOPs and ensure data integrity and traceability.
• Assist with department operations, paperwork, and documentation.
• Utilize GMP systems and maintain efficient testing workflows.

Skills

Detail-oriented

Communication skills

Teamwork

Microbiology knowledge

Troubleshooting

Education

Bachelor's degree in biology or relevant scientific discipline

Tools

Laser particle counters

Viable air samplers

Microscope

Endosafe Instrumentation

PCR

BacT/ALERT systems

Job description

POSITION SUMMARY

Schedule: Sun-Thu 2pm-11pm

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