Regulatory Affairs Associate — Cranial & Spinal Tech

Medtronic; Memphis (TN); On-site; USD 61,000 - 91,000; Full time

Job summary

Medtronic in Memphis, Tennessee, is seeking an Associate Regulatory Affairs Specialist to coordinate documentation, submissions, and regulatory records. This on-site role supports audits, inspections, and ongoing business operations, partnering across functions to ensure timely regulatory deliverables.

The position requires a bachelor’s degree with 1+ year in Regulatory Affairs or a regulated field, and proficiency in Microsoft Office and regulatory documentation practices.

Qualifications

• Bachelor's degree required.
• 1+ year of experience in Regulatory Affairs or a regulated environment.
• Knowledge of US and/or international regulatory requirements and documentation practices.
• Experience using Microsoft Office applications (Word, Excel, Outlook, PowerPoint).
• Experience using regulatory information management or document control systems.

Responsibilities

• Coordinate preparation and maintenance of regulatory submission packages.
• Gather materials for submissions, renewals, and registrations.
• Support audits, inspections, and regulatory inquiries with organized documentation.
• Review docs and update labeling, manufacturing processes, and marketing materials for compliance.
• Maintain systems tracking submissions, approvals, and records.
• Monitor regulatory guidance and changes to support ongoing compliance.
• Collaborate with cross-functional teams to complete regulatory deliverables on time.
• Assist with strategies and activities for obtaining and maintaining product approvals.

Skills

Regulatory submissions

Document control

US and international regulatory

Microsoft Office

Education

Bachelor's degree

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Regulatory information management systems

Quality management systems

Job description

Medtronic in Memphis, Tennessee, is seeking an Associate Regulatory Affairs Specialist to coordinate documentation, submissions, and regulatory records. This on-site role supports audits, inspections, and ongoing business operations, partnering across functions to ensure timely regulatory deliverables.

The position requires a bachelor’s degree with 1+ year in Regulatory Affairs or a regulated field, and proficiency in Microsoft Office and regulatory documentation practices.