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Kincell Bio

Cell therapy CDMO: development, CMC, manufacturing

Microbiology Technician 3 - Quality Control

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in microbiology, biology, or another relevant scientific discipline and at least 2 years of relevant microbiology laboratory experience, or at least 5 years of relevant microbiology laboratory experience in lieu of a degree.
  • Demonstrated experience performing environmental monitoring in a classified cleanroom or controlled environment.
  • Hands-on experience with aseptic gowning and working within classified cleanroom environments.
  • Demonstrated experience performing microbiological testing in a GMP-regulated, pharmaceutical, biotechnology, cell therapy, or similarly regulated environment.
  • Experience with applicable microbiological methods, including environmental monitoring, bioburden, bacterial endotoxin, microbial enumeration, growth promotion, Gram staining, subculture techniques, microbial identification, and/or sterility testing.
  • Experience with microbiological data analysis, trending, and technical report generation.
  • Demonstrated ability to work independently, exercise sound judgment, and complete assigned activities with minimal direct supervision.
  • Strong organizational, analytical, and problem-solving skills, with the ability to prioritize and manage multiple activities or projects simultaneously.
  • Ability to define problems, collect and evaluate data, establish facts, identify trends, and draw scientifically sound conclusions.
  • Strong attention to detail and commitment to accuracy, compliance, and data integrity.
  • Effective written and verbal communication skills, with the ability to communicate technical information clearly and professionally.
  • Demonstrated ability to adapt to a rapidly changing environment while maintaining quality, productivity, and compliance.
  • Proficiency with Microsoft Office applications and applicable laboratory information management systems.
  • Ability to work off-hours, weekends, or extended hours as required to support manufacturing and environmental monitoring activities.
  • Ability to wear required cleanroom and personal protective equipment, including full-body gowning, goggles, face shields, protective gloves, and other applicable personal protective equipment.

Responsibilities

  • Perform routine and non-routine environmental monitoring of classified cleanrooms and laboratory areas, including viable air, surface, personnel, compressed gas, and other applicable monitoring, in support of GMP manufacturing operations.
  • Perform environmental monitoring activities during off-hours, weekends, and other non-standard schedules as required to support manufacturing operations.
  • Serve as a senior technical resource for microbiology and environmental monitoring activities and provide guidance and support to other microbiology personnel as needed.
  • Perform critical utility microbiological monitoring in accordance with approved procedures, specifications, and established schedules.
  • Perform microbiological quality control testing of raw materials, in-process materials, and other applicable samples in accordance with approved procedures and GMP requirements.
  • Perform microbiological assays including bioburden, bacterial endotoxin, microbial enumeration, Gram staining, microbial identification, subculture techniques, plate reading, and other applicable microbiological methods.
  • Perform sterility testing, method verification, method suitability, and other microbiological testing activities as qualified, including use of automated microbial detection systems such as the BacT/ALERT 3D System.
  • Prepare microbiological media, buffers, reagents, and other laboratory materials in accordance with approved procedures.
  • Perform growth promotion testing and qualification of microbiological media in accordance with approved procedures and applicable compendial requirements.
  • Coordinate microbiological testing with external contract laboratories, including sample submission, test requirements, scheduling, result review, and reconciliation of final reports.
  • Manage and coordinate contract laboratory testing for environmental monitoring and other microbiological analyses, as assigned.
  • Perform routine data review, analysis, and trending of microbiological and environmental monitoring data and contribute to technical reports and scientifically sound conclusions.
  • Initiate and/or support environmental monitoring and microbiological assay investigations, including assessment of atypical results, alert/action level excursions, out-of-specification results, and other microbiological events.
  • Assist with root cause investigations, impact assessments, corrective actions, and effectiveness evaluations associated with microbiological events.
  • Assist with the qualification and validation of microbiology equipment, processes, facilities, and analytical methods, including protocol development, execution, data collection, and report generation.
  • Perform routine laboratory equipment maintenance, calibration activities, and troubleshooting as required.
  • Review laboratory data, worksheets, test records, and other controlled documentation for accuracy, completeness, and compliance with GMP and data integrity requirements.
  • Maintain the microbiology laboratory in a clean, organized, compliant, and inspection-ready condition.
  • Support laboratory readiness activities, including inventory management, preparation of laboratory supplies, and monitoring of media, reagents, and consumables.
  • Identify opportunities to improve microbiology laboratory processes, environmental monitoring practices, testing efficiency, and overall laboratory performance.
  • Train and provide technical guidance to less-experienced microbiology personnel on applicable laboratory procedures and microbiological techniques, as assigned.
  • Maintain proficiency in applicable microbiological methods and complete required training and competency assessments.
  • Comply with company policies, procedures, standard operating procedures, GMP requirements, applicable regulatory expectations, and data integrity principles.

Desired Qualifications

  • Experience with microbiology investigations, environmental monitoring excursions, atypical results, or out-of-specification events.
  • Experience supporting microbiology equipment, method, or process qualification and validation activities.

About the Company

Kincell Bio

Cell therapy CDMO: development, CMC, manufacturing

Kincell Bio is a CDMO that specializes in cell therapies, offering end-to-end development and manufacturing services for early-stage biotech companies and academic spinouts. It provides analytical development, process development, CMC consulting, and GMP manufacturing to advance autologous and allogeneic CAR-T, CAR-NK, and CAR-M programs from research through clinical trials. Led by experienced CDMO executives and supported by investors, it focuses on early-stage partnerships and has expanded capacity with a new RTP facility to scale mid- to late-stage studies. Its goal is to streamline the path from research to clinical trials and commercial production by delivering scalable, high-quality biomanufacturing and development services for the cell-therapy field.

Company size
51-200
Company stage
Early VC
Total funding
$58M
Headquarters
Gainesville, FL
Founded
2023

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