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

14 days+
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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.

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