Quality Management and Regulatory Affairs
Hourly rate: members only
Availability: members only
Willingness to travel: Europe
Professional status: Employer
Last updated: Mar 23, 2025
Total work experience:
Language skills: English, French,
Personal summary
I have been working with companies to comply with quality management and regulatory affairs requirements in the medical device (ISO 13485:2016, FDA & Health Canada) , aerospace (AS9100 & AS9120) , manufacturing and services industries (ISO 9001). The services provided are tailored to customer needs and can involve documentation, implementation, training and internal audits.
Language skills
English
Native speaker
French
Fluent knowledge