QC Micro Tech Lead - Temporary

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies.

We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.

For more information, please visit our website at

Kincell is seeking a highly motivated Microbiology Technician Lead who will be a key contributor to a dynamic and collaborative Quality Control team.

This Contract position will support the day-to-day activities of the manufacturing and quality control group by performing lot related and routine environmental monitoring of the clean rooms, microbial assay testing, maintenance of laboratory supplies, routine data trending, and coordination of samples to outside testing laboratories, and scheduling and managing technicians. Personnel will work in concert with and assist the manufacturing department and play a critical role in ensuring environmental control of the aseptic manufacturing facility.

Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of this position.

This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.

• Provide day-to-day technical support and lead-level guidance for microbiology laboratory and environmental monitoring activities supporting GMP manufacturing operations.
• Coordinate daily microbiology workload and assist in prioritizing environmental monitoring, QC testing, investigations, and other laboratory activities to ensure timely completion.
• Serve as a key technical resource and primary backup for microbiology and QC testing activities, maintaining proficiency in applicable microbiological and QC methods, including sterility, endotoxin, growth promotion, environmental monitoring, osmolality, pH and other applicable assays.
• Perform microbiological testing to support routine laboratory operations, manufacturing schedules, investigations, staffing requirements, and off-hours/weekend coverage as needed.
• Perform environmental monitoring activities, including viable air, surface, personnel, compressed gas, and other applicable monitoring within classified clean rooms and laboratory areas.
• Perform sterility testing, method verification, and method suitability activities, including testing using the BacT/ALERT 3D System.
• Perform routine operation, cleaning, maintenance, and troubleshooting of microbiology laboratory equipment and coordinate calibration and servicing as required.
• Assist with microbiology investigations, including environmental monitoring excursions, atypical results, out-of-specification results, and other microbiological events.
• Assist with root cause analysis, impact assessments, corrective actions, and effectiveness evaluations associated with microbiological investigations.
• Review microbiology records and analytical data for accuracy, completeness, compliance with procedures, and adherence to data integrity requirements.
• Serve as a technical resource to microbiology personnel and assist with troubleshooting laboratory methods, equipment, and testing activities.
• Assist in maintaining the microbiology laboratory in a clean, orderly, compliant, and inspection-ready condition.
• Collaborate with Quality Assurance, Manufacturing, Engineering, Validation, and other departments to support manufacturing operations, investigations, contamination control, and laboratory activities.
• Ensure all activities are performed in accordance with company policies, procedures, SOPs, GMP requirements, applicable regulatory expectations, and data integrity principles.

The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.

Required:

• Bachelor’s degree in microbiology, biology, or another relevant scientific discipline and a minimum of 2 years of relevant microbiology laboratory experience in a GMP-regulated environment.
• Demonstrated experience with environmental monitoring in classified cleanroom environments.
• Hands-on experience with aseptic gowning and working within classified cleanroom environments.
• Demonstrated proficiency in microbiological testing, including sterility, bacterial endotoxin, microbial enumeration, subculture techniques, environmental monitoring, osmolality, pH, etc.
• Demonstrated ability to provide technical leadership, mentoring, or…