General Submission - Life Sciences Consultant

🌍 Remote, USA 🚀 Full-time 🕐 Posted Recently

Job Description

    We are looking to connect with experienced consultants open to working now or on future assignments in cGMP pharmaceutical or biotech setting on assignments involving:
  • Compliance and Training
  • CSV & CFR Part 11
  • Data Integrity / Governance
  • Commissioning and Qualification
  • Quality System Implementation
  • Compliance ~ cGxP Consulting
  • Investigation and Deviation – CAPA
  • FDA Remediation
  • Audits and Assessments
  • Mock FDA Inspections
  • SOP / Policy Development
  • M&A Due Diligence
  • License Application Support

While we are headquartered in Sparta, NJ, we continually have a high number of consulting and contracting assignments on 1099 across the US.

A member of our Talent team will be in touch to discuss your application in more detail. In the meantime, check out our website: Home — Medvacon Life Sciences LLC

Quality Grind Podcast: Quality Grind Podcast — Medvacon Life Sciences LLC

Blog Series: Blog — Medvacon Life Sciences LLC

Important Notice: Protecting Your Information

Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to [email protected].

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