Job Description
Enhance quality processes at Vitaliti Technologies Inc. as a Quality and Regulatory Specialist in Kitchener, Ontario. This role focuses on maintaining ISO compliance and supporting regulatory documentation.
Vitaliti Technologies Inc. seeks a detail-oriented Quality and Regulatory Specialist to bolster processes in a regulated medical device environment. This position is perfect for professionals with 5+ years of experience who thrive in structured settings and excel in identifying documentation gaps. You'll collaborate with cross-functional teams to ensure compliance with standards and contribute to internal and external audits.
Key Responsibilities:
• Support communication with regulatory bodies in North America and EU
• Maintain internal quality processes like shipping and inspections
• Ensure QMS processes meet regulatory approval standards
• Assist in developing workflows and standards within QMS
• Perform gap analysis and update necessary documentation
Requ...
Vitaliti Technologies Inc. seeks a detail-oriented Quality and Regulatory Specialist to bolster processes in a regulated medical device environment. This position is perfect for professionals with 5+ years of experience who thrive in structured settings and excel in identifying documentation gaps. You'll collaborate with cross-functional teams to ensure compliance with standards and contribute to internal and external audits.
Key Responsibilities:
• Support communication with regulatory bodies in North America and EU
• Maintain internal quality processes like shipping and inspections
• Ensure QMS processes meet regulatory approval standards
• Assist in developing workflows and standards within QMS
• Perform gap analysis and update necessary documentation
Requ...