Nathan Majewski
CGT & Large Molecule Analytical Development, AS&T, QC, and Discovery
- Role
- Director, Qc at Iovance Biotherapeutics, Inc.
- Location
- Philadelphia, PA, US
- LinkedIn followers
- 500 followers
About Nathan Majewski
Analytical Development and QC: GLP assay development/qualification/validation, technology transfer (TT), analytical lifecycle management (LCM), and CMC for cell and gene therapy, large molecule, and medical device products• Management: 20 years of experience leading and developing teams of up to 30 scientists. Setting and maintaining departmental budget.• Regulatory Filings: experienced author of regulatory submissions (e.g. IND, BLA, RFD, 510k) and associated Information Requests (IRs)• Drug Discovery: 18 years industry experience in therapeutic large molecule, chimeric antigen receptor (CAR), and small molecule discovery• Collaboration: management of external collaborations with CROs, Biotechs, and academic labs• Project Leadership: leader of cross-functional target validation, therapeutic discovery, and analytical teams• Technical Expertise: breadth of knowledge in drug discovery, drug development, quality management, immunology, immune-oncology, cell & molecular biology, and statistical data analysis• Strategy: enterprise-wide thinker and matrix-leadership towards improved technical capabilities and workflows
Experience
Director, Qc
Mar 2025 — Present
Education
University of Illinois Chicago
Ph.D., Molecular Genetics
1998 — 2004
Penn State University
Bachelor of Science (B.S.), Biochemistry and Molecular Biology
1993 — 1997
Skills
- Drug Discovery
- Molecular Biology
- Assay Development
- Biotechnology
- Cell
- Life Sciences
- Biochemistry
- Cell Culture
- Antibodies
- Protein Chemistry
- Research
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