Todd Evans
Vice President of Quality and Regulatory Affairs at OsteoCentric Technologies
- Role
- Vice President of Quality and Regulatory Affairs at OsteoCentric Technologies
- Location
- Logan, UT, US
- LinkedIn followers
- 500 followers
About Todd Evans
I have over 29 years of experience in the medical device industry. I started my career in validation and quality engineering where I was directly involved in product development, supplier quality, complaint investigations, managing corrective and preventative actions, and sterilization processes. As a quality leader I have been involved in lean manufacturing, quality metric development, global harmonization, regulatory, and customer relations. I have a strong background in ISO13485, 21CFR 820, 21CFR 210, and 211. At one point of my career I have had the privilege to lead over 110 quality professionals across 5 global manufacturing sites. Currently I am responsible for Quality and Regulatory for OsteoCentric Technologies, where we develop a range of products for the Orthopedic, Dental and Veterinarian markets.
Experience
Vice President of Quality and Regulatory Affairs
May 2023 — Present · Logan, UT, US
Skills
- Gmp
- Quality System
- V&V
- Fda Gmp
- Iso
- Sop
- Fda
- Root Cause Analysis
- Cell Culture
- Technology Transfer
- 21 Cfr Part 11
- Medical Devices
- Capa
- Aseptic Technique
- Gamp
- Cleaning Validation
- Change Control
- Biopharmaceuticals
- Biotechnology
- Lean Manufacturing
- Iso 13485
- Chromatography
- Life Sciences
- Calibration
- Spc
- Sterilization
- Lifesciences
- Purification
- Quality Auditing
- Aseptic Processing
- Computer System Validation
- Fermentation
- Validation
- Cgmp Manufacturing
- Fmea
- Design Control
- Filtration
- Microbiology
- Continuous Improvement
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