Quality Control Analyst I & II (Microbiology)
Location: Memphis, TN
Duration: 6-Month Contract
Shift Options:
- Tuesday–Saturday, 2:00 PM – 11:00 PM
- Sunday–Thursday, 2:00 PM – 11:00 PM
Interview Process:
- 45-minute virtual interview
Pay Rates:
- QC Analyst I: $20.13 - $21.13/hour
- QC Analyst II: $22.50 - $24.50/hour
Position Summary
Quality Control Analyst I (QCI)
The QC Analyst I supports the Microbiology Department by performing routine environmental monitoring, product release testing, and raw material testing. This role requires strong attention to detail, organizational skills, computer proficiency, and a foundational understanding of microbiology and laboratory instrumentation. The ability to work independently in a fast-paced, highly regulated environment is essential.
Quality Control Analyst II (QCII)
The QC Analyst II performs more advanced microbiological testing, including environmental monitoring, sterility, and endotoxin testing. This role requires strong technical expertise, organization, and the ability to work with minimal supervision in a regulated laboratory environment.
Key Responsibilities
QC I Responsibilities
- Perform environmental monitoring (viable/non-viable air, surface, and personnel sampling)
- Receive and manage laboratory materials, supplies, and inventory
- Follow standard operating procedures (SOPs) and good documentation practices (GDP)
- Maintain lab documentation, logs, and filing systems
- Assist with laboratory organization and upkeep
- Utilize GMP systems (e.g., MODA) and other lab software
- Review test results for accuracy and ensure timely documentation
- Support overall laboratory operations
- Perform additional duties as assigned
QC II Responsibilities
- Conduct sterility and endotoxin testing for raw materials, in-process samples, and finished products
- Perform growth promotion testing of microbial media
- Execute environmental monitoring procedures
- Prepare excursion reports and assist with laboratory investigations
- Manage laboratory inventory and supplies
- Ensure compliance with SOPs and GDP for data integrity
- Support department operations, documentation, and inventory management
- Maintain knowledge of cGMP standards (CFR, USP, EP, ICH)
- Assist with lab organization and maintenance
- Review test results and ensure timely documentation for product release
- Perform additional duties as assigned
Qualifications
QC I Qualifications
- Bachelor’s degree in Biology or related scientific field required
- 0–2 years of laboratory experience or experience in cGMP/FDA-regulated environments
- Internship experience may be considered in lieu of professional experience
- Knowledge of microbiology and aseptic techniques
- Strong attention to detail and communication skills
- Ability to work independently or in a team
- Ability to work in a cleanroom environment with full gowning
- Problem-solving and troubleshooting skills
- Familiarity with lab equipment (e.g., particle counters, air samplers, microscopes, PCR, BacT/ALERT systems)
QC II Qualifications
- Bachelor’s degree (or higher) in Biological Sciences or related field required
- 1–2 years of relevant laboratory or cGMP/FDA-regulated industry experience
- Strong knowledge of microbiology and aseptic techniques
- Ability to work independently and collaboratively
- Ability to work in a cleanroom environment with full gowning
- Strong problem-solving and communication skills
- Detail-oriented with strong documentation practices
- Preferred: Experience with MODA, LIMS, or similar laboratory systems
- Preferred: Familiarity with laboratory instrumentation (particle counters, PCR, BacT/ALERT, etc.)
