General Submission - Life Sciences Consultant

Remote Full-time
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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