Qa/Ra Director - Bergamo

Job summary
QA/RA DirectorExciting Opportunity in Bergamo!Leading company in the medical device industry
Job seniority: director level and above
Responsibilities
• Identify unique regulatory requirements in new and existing markets• Assess the impact of regulations on manufacturing, product development, and the business• Propose solutions to address regulatory challenges• Manage practices for obtaining and maintaining certifications• Support the innovation unit in drafting technical specifications• Manage global product registrations and ensure compliance• Supervise the realization of user manuals and labeling information• Develop and manage the company's Quality and Environment system• Champion continuous improvement program• Maintain awareness of regulatory changes
Requirements
• Bachelor's degree in law, business administration, or engineering• 10 years of experience in similar roles or medical device development• Good knowledge of quality management standards, medical device regulations, and ISO requirements• Strong project management skills• Exceptional communication skills• Fluent in Italian and English
Benefits
• Opportunity to work in a leading company in the medical device industry• Contribute to the growth and success of the organization• Competitive salary and benefits package