Hillary Hillmann
Director of Quality Control, Cell & Gene Therapy Biologics CDMO
- Role
- Director of Quality Control at Cellectis
- Location
- Raleigh, NC, US
- LinkedIn followers
- 500 followers
About Hillary Hillmann
15 years of experience in biotechnology and research; 10 years in a GMP/CDMO Quality unit specializing in cell and gene therapy biologics. Expertise in method validation, specification establishment, release testing, and stability program administration for drug substance and drug product therapeutics for Phase I, II, and commercial clients. Knowledgeable in GMP, GLP, GDP, ICH, CFR, and USP Guidelines. Experience with EtQ Reliance, Documentum, SmartSolve, Master Control, TrackWise, MODA, and LabWare LIMS systems.
Experience
Director of Quality Control
Mar 2025 — Present · Raleigh-Durham-Chapel Hill, NC, US
Education
University of Florida
Master of Science (M.S.), Entomology, Biochemistry
2010 — 2013
Virginia Tech
Bachelor of Science (B.S.), Biology, Chemistry
2005 — 2009
Skills
- Research
- Quality Control
- Biology
- Biochemistry
- Entomology
- Chemistry
- Gmp
- Glp
- Pcr
- Cell Culture
- Pipetting
- Elisa Assays
- Dna and Rna Extraction
- Flow Cytometry
- Animal Handling
- Protocol Development
- Assay Qualification
- Gel Electrophoresis
- Elisa
- Animal Work
- Dna
- Western Blotting
- Life Sciences
- Laboratory
- Biotechnology
- Molecular Biology
- Assay Development
- Sop
- Microbiology
- Science
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