Join the GxP Source Expert Network

Connect with Life Sciences Organizations Sourcing Independent Auditors, QMS Consultants & Regulatory Strategists

GxP Source matches pharmaceutical, biotechnology, and medical device organizations with qualified independent consultants and experts for mock inspections, gap assessments, validation / quality assurance, technical writing, research, business development, regulatory remediation, and more.

Listing your profile in our directory places your specialized capabilities directly in front of directors and executive decision-makers actively seeking external expertise.

Why List Your Profile on GxP Source?

  • Targeted Visibility: Reach biopharma and medtech sponsors actively seeking specialized audit and compliance support.
  • Direct Client Inquiries: Prospective clients contact you directly—no hidden intermediary commissions or platform brokerage fees.
  • Verified Authority: Showcase your certifications (ASQ CQA, RAC, CQE), former agency experience, and core skills.

Who Can Apply?

We welcome independent consultants, lead auditors, and advisory firms with demonstrated domain expertise in:

  • GMP & Manufacturing QA (Facility audits, supplier qualification, QMSR transition, sterile manufacturing)
  • Validation & Digital Compliance (CSV/CSA, 21 CFR Part 11, Data Integrity, MES, LIMS)
  • Audits, Inspections & Remediation (FDA 483 response, Warning Letter remediation, mock inspections)
  • Clinical & Laboratory (GCP trial audits, CRO oversight, GLP analytical lab compliance)
  • Regulatory Affairs & Strategy (510(k), PMA, IND/NDA filings, CE marking, EU MDR)
woman in a lab coat in a lab looking into a microscope.

How to Submit Your Profile

To be listed in the directory, please email your profile details to our editorial team at info@gxpsource.com with the following information:

  1. Full Name & Professional Credentials (e.g. Jane Doe, ASQ CQA, RAC)
  2. Location & Travel Availability (e.g. Boston, MA, USA / Global & Remote)
  3. Primary Specializations (e.g. Biotech Business Development, GMP Mock Audits, Data Integrity)
  4. Professional Summary (A 2–3 paragraph bio highlighting your years of experience, past agency background if applicable, and typical client engagements)
  5. Contact Information (Email, Phone, Website, and LinkedIn Profile URL)
  6. Professional Headshot or Business Logo (High-resolution PNG or JPG attachment)