David Laudeman
Solution-oriented biotech leader skilled in GMP, validation, and quality driving efficient execution. I empower teams through supportive, collaborative leadership that delivers consistent results.
- Role
- Associate Director Cqv at Humacyte
- Location
- Durham, NC, US
- LinkedIn followers
- 500 followers
About David Laudeman
I have led teams through a variety of validation and quality projects of increased complexity to meet aggressive timelines. Expert in leadership, communication, cross-functional collaboration and problem-solving. Proven track record managing end-to-end validation and quality projects including project planning, timeline, team performance, project tracking, reporting, documentation and stakeholder management. Passionate about building productive and happy teams with a focus on coaching, career development and goal setting. Additional Training: Certified \"Licensed to Coach\" People management tool\"Playing to Win\" 6 part series on effective people managementBiopharmaceutical Quality Operations – Quality Assurance Services cGMP Training and Certification.November of Maryland, Baltimore County Biotechnology GMP Facility Design, Construction and Validation. January - May and Computrain, Frederick, MD 21702Intro and Intermediate Microsoft Excel University of Maryland, Baltimore CountyRegulatory Issues in Biotechnology.September of Maryland, Baltimore County Quality Control and Quality Assurance for Biotechnology Products August State University, State College, PAPenn State Biotechnology Training ProgramSeparation and Purification Strategies for Biotechnology Products, June 20-23, Pharmacia BiotechPiscataway, New JerseyLarge Scale Column Packing (Col 1)July 16–18, 2001Frederick Community CollegeFrederick MDCustomer Service TrainingSeptember 2004Annual Asbestos trainingOn site training in building 54•••04, 2005, 2006, 2007.
Experience
Associate Director Cqv
Mar 2025 — Present · US
Education
Commonwealth University-Lock Haven
BS, Environmental Biology
1986 — 1991
Skills
- Biotechnology
- Manufacturing
- 21 Cfr Part 11
- Sop
- Fda
- Quality Control
- Gmp
- Technology Transfer
- Life Sciences
- Biopharmaceuticals
- Aseptic Processing
- Quality Assurance
- Validation
- Lims
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