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 bolthires 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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