Quality Control Laboratory Technician
Quality Control Analyst I
Location: Bogart, GA
Duration: 12 Months Contract
Work Schedule: 100% Onsite, Laboratory-Based Role
Interview Process: Initial Screening Interview + Onsite Interview
Position Summary
We are seeking a Quality Control Analyst I to support commercial and clinical manufacturing activities within the QC Microbiology laboratory. This role is responsible for performing microbiological testing, supporting laboratory operations, maintaining compliance with cGMP requirements, and ensuring accurate documentation of all testing activities.
The ideal candidate will have a Bachelor’s degree in Biology, Microbiology, or a related scientific discipline and hands-on experience with microbiological testing techniques in a GMP-regulated laboratory environment.
Key Responsibilities
• Perform microbiological testing including:
• Bioburden Testing
• Endotoxin Testing
• Microbial Identification
• Growth Promotion Testing
• Support Environmental Monitoring and Utility Monitoring activities.
• Assist with product testing, laboratory qualifications, and investigations as needed.
• Identify and report abnormal test results or sample conditions to laboratory management.
• Prepare and compile investigation documentation.
• Follow established SOPs and cGMP requirements.
• Maintain accurate, complete, and legible laboratory records.
• Prepare reagents, media, and laboratory solutions.
• Clean, maintain, and support laboratory equipment and instrumentation.
• Order, receive, label, log, and maintain laboratory inventory and supplies.
• Participate in training activities and maintain current training records.
• Train laboratory personnel in assigned areas of expertise.
• Support laboratory documentation review activities as assigned.
Required Qualifications
• Bachelor’s degree in Biology, Microbiology, or a related scientific discipline.
• 0-2 years of experience in a QC Microbiology laboratory environment.
• Knowledge of cGMP regulations and laboratory documentation practices.
• Experience working in a regulated pharmaceutical, biotechnology, or life sciences environment.
• Strong written and verbal communication skills.
• Ability to follow detailed procedures and work with minimal supervision.
Required Technical Skills
• Aseptic Technique
• Bioburden Testing
• Endotoxin Testing (LAL)
• Microbial Identification
• Growth Promotion Testing
• Environmental Monitoring
• Media Preparation
• Cell Culture Techniques
• Laboratory Documentation
• GMP/cGMP Compliance
Preferred Qualifications
• Experience supporting commercial or clinical manufacturing operations.
• Experience with cleanroom environments and microbiology laboratory operations.
• Experience writing or supporting laboratory investigations.
• Familiarity with utility monitoring and qualification activities.
• Experience troubleshooting microbiological assays and laboratory instrumentation.
Key Competencies
• Strong attention to detail
• Organizational and time-management skills
• Problem-solving and troubleshooting abilities
• Ability to work independently and collaboratively
• Commitment to quality and compliance
• Effective verbal and written communication skills
Work Environment
• 100% onsite laboratory position.
• Work performed in a QC Microbiology laboratory supporting manufacturing operations.
• Regular interaction with laboratory equipment, microbiological testing materials, and cleanroom environments.
Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
Quality Assurance, Research, and Science
Contract