QC Analyst I-Microbiology

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

Job summary

Planet Pharma in Memphis, TN seeks a Quality Control Analyst I for the QC Microbiology Department. Schedule: Sun-Thu 2pm-11pm. You will perform environmental monitoring, raw material testing, and product-release testing with careful data integrity.

Requires a biology degree and 0-2 years lab experience, GMP familiarity, and strong written/verbal communication. You will use microbiology instrumentation and maintain documentation.

Qualifications

• Bachelor's degree in biology or relevant scientific discipline.
• 0–2 years of lab experience in GMP or FDA-regulated environment preferred.
• Internship program possible for lesser education/experience.
• Clean Room gowning required and ability to work in clean room.
• Ability to work independently or as part of a team.
• Detail-oriented with strong written and verbal communication.
• Knowledge of microbiology and aseptic techniques.
• Troubleshooting and problem-solving abilities.
• Familiarity with lab instrumentation and related equipment.

Responsibilities

• Perform environmental monitoring (air, surface, and personnel).
• Handle raw materials and inventory for QC lab, maintaining supplies.
• Follow SOPs and gDOC practices to ensure data integrity.
• Support department operations, logs, and documentation.
• Assist with routine lab upkeep and organization.
• Utilize GMP systems (MODA and related software).
• Review peers' test results and ensure timely release documentation.
• Comply with cGMP guidelines and training requirements.
• Perform additional related duties as assigned.

Skills

Detail-oriented

Written and verbal communication

Independent work

Microbiology knowledge

Aseptic techniques

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