Cyril Chaput Email
Senior Quality Assurance Manager, Product Devlt @ Kinova
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Cyril Chaput Location
- Montreal, QC, CA
Cyril Chaput Work
- Senior Quality Assurance Manager, Product Devlt @ (April 2026 - Present)
- VP, Regulatory Compliance and Quality Assurance @ (January 2011 - Present)
- Consultant, Systems Designer, ROSA CT Hip Pre-Operative Planning system. @ (October 2025 - February 2026)
- Manager, Quality and Regulatory (QA and RA) @ (September 2022 - August 2025)
- Director Quality Assurance @ (June 2016 - September 2017)
- Vice-president, Quality Assurance and Regulatory Affairs @ Infitrak Inc (now part of MESA LABS) (January 2011 - January 2016)
- Cold Supply Chain Compliance Specialist, Director of Marketing @ Alternatives Technologie Pharma Inc. (now part of TCP Reliable/Cryopak) (July 2005 - March 2010)
- Scientific Advisor @ Validapro Inc. / Pharma-Concept Inc. (January 2003 - January 2005)
- Director, Business Devlt and IP and Project leader @ Angiogene Inc. (January 2001 - January 2003)
- Director, IP @ BioSyntech (January 1996 - January 2001)
- Director, Bone Products Development @ BioSyntech (January 1996 - January 2001)
- Senior Scientist @ BioSyntech (January 1996 - January 2001)
Cyril Chaput Education
- University of Quebec
MBA (Bio-industries Management)
2001-2003 - Polytechnique Montréal
PhD (Biomedical Eng)
1992-1995 - Université Laval
M.Sc. (Exp. Medicine)
1989-1992
Cyril Chaput Skills
- Compliance Regulations
- International Regulations
- Software Testing
- Regulatory Submissions
- Software Quality Assurance
- Global Regulatory Compliance
- Validation Master Plans
- Qualification Testing
- Process Qualification
- Technical Writing
- Written Communication
- Project Support
- Bilingualism
- Regulatory Approvals
- Regulatory Strategy
- Change Management
- Risk Management
- Medical Device Success Platform
- ISO 22442
- Common Technical Document (CTD)
- Medical Device Directive
- Medical Device Regulation (MDR)
- TGA
- CMDR
- ASEAN
- Regulatory Compliance
- Aseptic Technique
- Sterile Processing
- Injectable Fillers
- Research and Development (R&D)
- Quality Management
- Medical Devices
- Biotechnology
- Compliance
- Intellectual Property
- Supply Chain
- Life Sciences
- Lifesciences
- Quality System
- Validation
- GMP
- ISO 13485
- Quality Assurance
- Biopharmaceuticals
- Product Development
- FDA
- Pharmaceutical Industry
- Regulatory Affairs
- Pharmaceutics
- BPF
- Management
- Design Control
- MDSAP
- Corrective and Preventive Action (CAPA)
- Standard Operating Procedure (SOP)
- Development
- Networking
- Data Validation
- Regulatory
- Injectable
- Quality Systems
Cyril Chaput Summary
- Cyril Chaput, based in Montreal, QC, CA, is currently a Senior Quality Assurance Manager, Product Devlt at Kinova. Cyril Chaput brings experience from previous roles at Oligo Medic, Zimmer CAS, Statera Medical and SoundBite Medical Solutions Inc.. Cyril Chaput holds a 2001 - 2003 MBA in Bio-industries Management @ University of Quebec. With a robust skill set that includes Compliance Regulations, International Regulations, Software Testing, Regulatory Submissions, Software Quality Assurance and more. Cyril Chaput has 3 emails on RocketReach.
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