Dan Marsteller
Director- GMP Facilities at Precigen
- Role
- Director- Gmp Facilities at Precigen
- Location
- Germantown, MD, US
- LinkedIn followers
- 500 followers
About Dan Marsteller
A motivated and energetic leader, I enjoy process improvement, system building, and problem solving. Witnessing the positive impact of my contribution is one of the main drivers of my work. I aim to increase my influence through the multiplicative effect of compelling servant leadership, enabling the entire team to succeed.Bucknell’s Biomedical Engineering coursework focused on innovative product development and engineering fundamentals. My professional experience in developmental, clinical, and commercial biotechnology, animal health, and pharmaceutical companies spans quality, operational excellence, project management, engineering, facilities, validation, and manufacturing science / technology departments on both sides of the CDMO relationship. Throughout my career I have sought certifications to complement my experience with additional training on process improvement, project management, and safety. Johns Hopkins Carey Business School’s MBA and Management Development Certificate coursework increased my understanding of business drivers and built on my available toolkit to drive the success of my team. My mentors and supervisors praise my learning agility, high work capacity, and willingness to embrace a challenge. This experience and my passion position me well to provide exponential value increases in any life science organization.I am always interested in connecting with others who share my enthusiasm. Feel free to reach out through LinkedIn or via email at d••••••••@gmail.com.Specialties: Leadership, Process Improvement, System Development, Quality Systems, Problem Solving, Team Builing and Development, Facility Management, Safety
Experience
Director- Gmp Facilities
Jun 2024 — Present · Germantown, MD, US
Strategic and operational leadership of Precigen GMP manufacturing facilitiesLead commercialization of GMP Manufacturing and Quality Control facilities including capital upgrades and GMP system updates for enhanced compliance, while improving efficiency and effectiveness of support systems.Ensure proper Facility, Utility, and Equipment operation through enhanced maintenance systems. Drive compliance and system suitability via Validation and Metrology process update and execution. Build improved safety culture with increased formality of safety program.
Education
Bucknell University
Bachelor of Science, Biomedical Engineering
2007 — 2011
The Johns Hopkins University - Carey Business School
Master of Business Administration - MBA
2017 — 2020
The Johns Hopkins University - Carey Business School
Management Development Certificate, Business Administration, Management and Operations
2021 — 2023
Skills
- Biomedical Engineering
- Process Improvement
- Six Sigma
- Root Cause Analysis
- Creative Problem Solving
- Adaptability
- Process Engineering
- Biomedical Device Design
- Pharmaceutical Industry
- Fmea
- Medical Devices
- Analysis
- Validation
- Pharmaceutical Manufacturing
- Cgmp Practices
- Cgmp Manufacturing
- Gmp
- Solidworks
- Minitab
- Labview
- Fda
- Research
- Testing
- Chemistry
- Mass Spectrometry
- Hplc
- Matlab
- Scanning Electron Microscopy
- Microsoft Office
- Microsoft Excel
- Microsoft Word
- Project Management
- Corrective and Preventive Action (Capa)
- Technical Investigations
- Deviation Management
- Process Validation
- Change Control
- Microsoft Project
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