General Submission - Life Sciences Consultant

Medvacon Life Sciences, LLC

Sparta, NJ

JOB DETAILS
SKILLS
Biology, Biotech and Pharmaceutical, Blog, Consulting, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Data Quality, FDA (Food and Drug Administration), GCP (Good Clinical Practices), GxP, Podcasting, Policy Development, Software Administration, Standard Operating Procedures (SOP)
LOCATION
Sparta, NJ
POSTED
30+ days ago

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.

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About the Company

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Medvacon Life Sciences, LLC