General Submission - Life Sciences Consultant

Remote, USA 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 SupportWhile 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 LLCQuality Grind Podcast: Quality Grind Podcast — Medvacon Life Sciences LLCBlog Series: Blog — Medvacon Life Sciences LLCImportant Notice: ProtectingYour InformationMedvacon 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] tot his job
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