Quality Control Manager-Department of Neurosurgery-GMP Lab

JOB NO:

539849

WORK TYPE:

Staff Full-Time

LOCATION

Main Campus (Gainesville, FL)

CATEGORIES

Biology/Life Science, Office/Administrative/Fiscal Support, Health Care Administration/Support

DEPARTMENT

29190000 - MD-NEUROLOGICAL

SURGERY CLASSIFICATION TITLE

Research & Development Manager

CLASSIFICATION MINIMUM REQUIREMENTS

Master's degree in an appropriate area and seven years of relevant experience.

JOB DESCRIPTION

QC Laboratory Operations & Compliance Lead day-to-day operations of the QC laboratory in support of in-process, release, and stability testing for GMP clinical materials. Author, revise, and implement SOPs, specifications, forms, protocols, reports, and laboratory documentation to maintain a robust and scalable QC system. Review and approve laboratory records, test results, logbooks, worksheets, protocols, reports, and other controlled documentation for completeness, accuracy, and compliance. Lead or support laboratory investigations related to OOS, OOT, deviations, atypical results, excursions, and CAPA Support method qualification, transfer, validation readiness, and new assay implementation as programs evolve. Team Leadership & Lab Oversight Supervise QC staff, including training, scheduling, workload prioritization, performance management, and technical development. Support the environmental monitoring program for classified GMP spaces, including scheduling, trend review, documentation, and collaboration with Facilities and QA on excursions and corrective actions. Oversee laboratory equipment readiness, maintenance, calibration, qualification, and troubleshooting coordination to ensure an inspection-ready QC operation. Cross-Functional Collaboration Partner closely with Manufacturing, Facilities, and Quality Assurance to align testing priorities with production schedules, investigations, batch disposition needs, and facility monitoring requirements.

EXPECTED SALARY

$96,350-$110,700 REQUIRED

QUALIFICATIONS

Master's degree in an appropriate area and seven years of relevant experience.

PREFERRED

Working knowledge of cGMP, GLP, GDP, deviation management, investigations, CAPA, change control, and data integrity principles. Minimum 5-8 years of relevant experience in a GMP-regulated biopharmaceutical, biotechnology, cell therapy, gene therapy, or CDMO environment, including progressive QC laboratory responsibilities. Prior experience supporting cell therapy, gene therapy, immunotherapy, or other advanced therapy products. Hands-on experience with cell-based assays, flow cytometry, PCR/qPCR, molecular assays, sterilityrelated testing support, and/or potency-related assay Experience with environmental monitoring in classified cleanroom environments. Experience with method transfer, qualification, validation support, and assay lifecycle management. Prior experience supervising or mentoring laboratory personnel Excellent attention to detail and commitment to data integrity; Strong written and verbal communication skills

SPECIAL INSTRUCTIONS TO APPLICANTS

For consideration, please complete an application and include a cover letter, resume and the names and email addresses of three to five references. The University of Florida is an Equal Employment Opportunity Employer. Application must be submitted by 11:55 p.m. (ET) of the posting end date.

HEALTH ASSESSMENT REQUIRED

Yes

ADVERTISED

08 May 2026 Eastern Daylight Time

APPLICATIONS CLOSE

22 May 2026 Eastern Daylight Time