Regulatory Affairs Consultant — Medical Devices & Pharma

MedCepts Medical Sales & Marketing Network - Medical Devices / Pharmaceuticals; Nashville (TN); On-site; USD 90,000 - 193,000; Full time

Job summary

MedCepts Medical Sales & Marketing Network - Medical Devices / Pharmaceuticals is seeking independent consultants with experience in Regulatory Affairs for medical products, medical equipment, devices, and biologics.

The role covers strategy, submission preparation, document creation, and post-approval support for projects in the USA and globally, with fee-based contract opportunities across the life sciences sector.

Qualifications

• Experience in regulatory affairs for medical products.
• Ability to prepare and submit regulatory documents.
• Experience with US FDA processes and global approvals.
• Contract-based consulting in life sciences.

Responsibilities

• Strategy, preparation and submission
• Document preparation
• Approval Support
• Strategic Advice
• Approval Process
• Post approval support
• Investigational
• USA
• Global

Skills

Regulatory Affairs

Documentation

Strategic submissions

Life sciences

Job description

MedCepts Medical Sales & Marketing Network - Medical Devices / Pharmaceuticals is seeking independent consultants with experience in Regulatory Affairs for medical products, medical equipment, devices, and biologics.

The role covers strategy, submission preparation, document creation, and post-approval support for projects in the USA and globally, with fee-based contract opportunities across the life sciences sector.