M
General Submission - Life Sciences Consultant
medvacon
Remote
15h ago
97%
Strong
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 jobs@medvacon.com.