Dan Dillon Location
- West Lafayette, IN, US
Dan Dillon Work
- 2016 - now Senior Regulatory Scientist @
- 2006 - 2016 Regulatory Scientist @
- 2005 - 2006 Manager, Regulatory Affairs @ Stryker Biotech
- 2002 - 2005 Staff Consultant @ Medical Device Consultants Inc. (MDCI)
- 1999 - 2002 Director, Regulatory Affairs @
- 1988 - 1999 Regulatory Affairs Project Manager @
- 1995 - 1998 Senior Regulatory Affairs Specialist @
- 1994 - 1995 Regulatory Affairs Specialist @
- 1992 - 1994 Regulatory Affairs Associate @ American Sterilizer Company (Amsco)
- 1989 - 1992 Regulatory Affairs Coordinator @ Olympus Corporation
- 1988 - 1989 Applications Engineer @ Olympus Corporation
- 1986 - 1988 Project Engineer @
Dan Dillon Education
- Purdue University
M.S.
2007 - 2010 - Rose-Hulman Institute of Technology
B.S. Chemicial Engineering (Chemical Engineering w/ Chemistry as Second Major)
1980 - 1984
Dan Dillon Skills
- FDA
- Medical Devices
- Regulatory Affairs
- Biomedical Engineering
- V&V
- GMP
- Lifesciences
- R&D
- Biotechnology
- Clinical Trials
- Sop
- ISO 13485
- Regulatory Submissions
- Design Control
- Pharmaceutical Industry
- GCP
- GLP
- Quality System
- Clinical Research
- Validation
- Clinical Development
- CAPA
- Regulatory Requirements
- 21 CFR Part 11
- Quality Auditing
- ISO 14971
- Quality Assurance
- Change Control
- Combination Products
- Biocompatibility
- PMA
- CRO
- Regulatory Strategy Development
Dan Dillon Summary
- Dan Dillon, based in West Lafayette, IN, US, is currently a Senior Regulatory Scientist at MED Institute. Dan Dillon brings experience from previous roles at MED Institute, Stryker Biotech, Medical Device Consultants Inc. (MDCI) and Waters Corporation. Dan Dillon holds a 2007 - 2010 M.S. @ Purdue University. With a robust skill set that includes FDA, Medical Devices, Regulatory Affairs, Biomedical Engineering, V&V and more. Dan Dillon has 2 emails on RocketReach.
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West Lafayette, IN, US
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West Lafayette, IN, US
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West Lafayette, IN, US
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