Adam Veller
Senior Manager, Quality Assurance: Technology Transfer, New Product Introduction, RFT GMP Production, Validation
- Role
- Senior Quality Assurance Manager-technical Quality Lead at OXB
- Location
- Fayetteville, NC, US
- LinkedIn followers
- 500 followers
About Adam Veller
As the Technical Manager of Quality, the focus through leadership is on enabling successful technical and analytical transfers, ensuring cGMP compliance, Right First-Time (RFT) execution and embedding Quality by Design principles into clinical production processes for client products. For lifecycle \"mature\" products, the focus is on successful RFT execution of Process Performance Qualifications and the compliant validation of all associated equipment and processes. Expertise spans technology transfer, analytical method transfers, purification, and scale-up, from development to commercial/validated, ensuring all products meet rigorous quality standards while supporting seamless execution. As an individual contributor, I developed extensive hands-on experience in chromatography method development and validation. By fostering cross-functional alignment, I was able to drive operational excellence, ensuring technical transfers, chromatography operations and production met strategic goals and delivered impactful solutions to patients worldwide.
Experience
Senior Quality Assurance Manager-technical Quality Lead
Jan 2026 — Present · US
Education
Illinois State University
Bachelor of Science - BS, Biology/Biological Sciences, General
Illinois State University
Bachelors of Science in Biology, Chemistry minor
1988 — 1992
Skills
- Hplc
- Column Chromatography
- Cell Culture
- Lifesciences
- Purification
- Filtration
- Technology Transfer
- Gxp
- Aseptic Processing
- Validation
- Biochemistry
- Aseptic Technique
- Pharmaceutical Industry
- Sop
- Fda
- Gmp
- Drug Discovery
- Protein Chemistry
- Capa
- Clinical Development
- Fermentation
- Ind
- Lims
- Manufacturing
- Cgmp
- Glp
- Cleaning Validation
- V&V
- Process Simulation
- Formulation
- Elisa
- Change Control
- Cell
- Vaccines
- Microbiology
- Drug Development
- Biopharmaceuticals
- Regulatory Submissions
- 21 Cfr Part 11
- Computer System Validation
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