Senior Regulatory Affairs Specialist - Medical devices

Summary: The Senior Regulatory Affairs Specialist for Medical Devices is responsible for ensuring compliance with regulatory requirements in the medical device industry. This role involves managing submissions and maintaining regulatory documentation while working remotely. The position is classified as outside IR35, indicating a flexible working arrangement.

Key Responsibilities:

• Ensure compliance with regulatory requirements for medical devices.
• Manage submissions and maintain regulatory documentation.
• Collaborate with cross-functional teams to support product development.
• Monitor changes in regulations and assess their impact on the organization.

Key Skills:

• Strong knowledge of regulatory requirements for medical devices.
• Experience in managing regulatory submissions.
• Excellent communication and collaboration skills.
• Ability to analyze and interpret regulatory changes.

Salary (Rate): undetermined

City: undetermined

Country: USA

Working Arrangements: remote

IR35 Status: outside IR35

Seniority Level: undetermined

Industry: Other