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Komline-Harn

General Submission - Life Sciences Consultant

RemotePosted 1 weeks ago
onsite

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].

General Submission - Life Sciences Consultant at Komline-Harn | Renata